accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other CYP2A6 CNV Assays ›
Gene Symbol
CYP2A6
Assay Reference Genome
Location

Chr.19:40849456 on build GRCh38
Cytoband
19q13.2
Assay ID Hs04488984_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 1548

Gene Name:

 cytochrome P450 family 2 subfamily A member 6

Gene Aliases:

 CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB

Location:

 Chr.19:40843538-40850447 on Build GRCh38

Assay Gene Location:

 Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
CYP2A6 NM_000762.5 NP_000753.3
AF182275.1 AAF13600.1
AK307740.1
AK309594.1
AK312964.1
BC096253.3
BC096254.1 AAH96254.1
BC096255.1 AAH96255.1
BC096256.1 AAH96256.1
DA641580.1
M33318.1 AAA52067.1
X13897.1 CAA32097.1
X13929.1 CAA32117.1
X13930.1 CAA32118.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1065886 Chr.19:40833952 - 40891756 on Build GRCh38 Loss CYP2A7 CYP2A6 CYP2G1P
nsv438302 Chr.19:40848628 - 40868128 on Build GRCh38 Loss CYP2A6
esv2760509 Chr.19:40819099 - 40888431 on Build GRCh38 Gain+Loss CYP2A7 CYP2A6
esv3644362 Chr.19:40848147 - 40867633 on Build GRCh38 Loss CYP2A6
esv3893202 Chr.19:40844990 - 40878673 on Build GRCh38 Gain+Loss CYP2A7 CYP2A6
nsv1056244 Chr.19:40823313 - 40891756 on Build GRCh38 Gain CYP2A7 CYP2A6 CYP2G1P
nsv442765 Chr.19:40845089 - 40875041 on Build GRCh38 Gain+Loss CYP2A6
dgv3535n100 Chr.19:40839241 - 40865028 on Build GRCh38 Gain+Loss CYP2A6
nsv435697 Chr.19:40848417 - 40882223 on Build GRCh38 Deletion CYP2A7 CYP2A6
esv2763010 Chr.19:40828833 - 40875041 on Build GRCh38 Gain+Loss CYP2A6
dgv588n67 Chr.19:40848914 - 40867881 on Build GRCh38 Loss CYP2A6
dgv1046e212 Chr.19:40839410 - 40886237 on Build GRCh38 Gain CYP2A7 CYP2A6
dgv3537n100 Chr.19:40842952 - 40865028 on Build GRCh38 Loss CYP2A6
nsv579545 Chr.19:40848724 - 40875596 on Build GRCh38 Gain CYP2A7 CYP2A6
nsv1066637 Chr.19:40803306 - 41091991 on Build GRCh38 Gain EGLN2 CYP2B6 CYP2T1P CYP2A13 CYP2A7 CYP2B7P CYP2A6 CYP2G1P RAB4B-EGLN2 CYP2A7P1
esv33053 Chr.19:40834724 - 40894730 on Build GRCh38 Gain CYP2A7 CYP2A6 CYP2G1P
dgv642e199 Chr.19:40838625 - 40869922 on Build GRCh38 Deletion CYP2A6
esv3893206 Chr.19:40835684 - 40859190 on Build GRCh38 Gain+Loss CYP2A6
dgv142n111 Chr.19:40833964 - 40888431 on Build GRCh38 Deletion CYP2A7 CYP2A6
nsv817836 Chr.19:40827379 - 40857860 on Build GRCh38 Gain+Loss CYP2A6
esv2718568 Chr.19:40834053 - 40875511 on Build GRCh38 Deletion CYP2A7 CYP2A6
nsv433318 Chr.19:40845362 - 40859190 on Build GRCh38 Loss CYP2A6
dgv1045e212 Chr.19:40839255 - 40870102 on Build GRCh38 Gain CYP2A6
nsv482219 Chr.19:40843538 - 40850447 on Build GRCh38 Gain CYP2A6
dgv3531n100 Chr.19:40828821 - 40875029 on Build GRCh38 Loss CYP2A6
dgv1048e212 Chr.19:40846721 - 40870102 on Build GRCh38 Loss CYP2A6
esv3584737 Chr.19:40839253 - 40875041 on Build GRCh38 Loss CYP2A6
esv2758762 Chr.19:40785722 - 41040163 on Build GRCh38 Gain+Loss EGLN2 CYP2B6 CYP2T1P RAB4B CYP2A7 MIA-RAB4B CYP2B7P CYP2A6 CYP2G1P RAB4B-EGLN2 CYP2A7P1
esv3644361 Chr.19:40846558 - 40877202 on Build GRCh38 Loss CYP2A7 CYP2A6
dgv3533n100 Chr.19:40832930 - 40875029 on Build GRCh38 Gain+Loss CYP2A6
nsv1160623 Chr.19:40842964 - 40863500 on Build GRCh38 Deletion CYP2A6
nsv9729 Chr.19:40831900 - 40888502 on Build GRCh38 Loss CYP2A7 CYP2A6
dgv6444n54 Chr.19:40844134 - 40866570 on Build GRCh38 Loss CYP2A6
esv3893205 Chr.19:40843869 - 40850594 on Build GRCh38 Loss CYP2A6
dgv6442n54 Chr.19:40843827 - 40887855 on Build GRCh38 Loss CYP2A7 CYP2A6
esv21610 Chr.19:40831396 - 40887351 on Build GRCh38 Gain+Loss CYP2A7 CYP2A6
nsv963049 Chr.19:40846083 - 40854024 on Build GRCh38 Duplication CYP2A6
nsv2490 Chr.19:40834142 - 40867364 on Build GRCh38 Insertion CYP2A6
nsv1061439 Chr.19:40846466 - 40863792 on Build GRCh38 Gain CYP2A6

Back To Top

More Information


Important Information

Individuals may carry null alleles or extra copies of CYP2A6. Some CYP2A6 alleles contain sequences derived from the highly homologous CYP2A7 pseudogene. Hs04488984_cn specifically targets CYP2A6 intron 2 sequences and will not amplify CYP2A7, but will amplify CYP2A6/CYP2A7 hybrid alleles carrying CYP2A6 intron 2 sequences (e.g. CYP2A6*12 contains CYP2A7 exons 1-2 and CYP2A6 exons 3-9).

Additional Information:

Set Membership:

 Intragenic Intronic Non-exonic DGV Variation Validated

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products