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See other AHNAK2 CNV Assays ›
Gene Symbol
AHNAK2
Assay Reference Genome
Location

Chr.14:104941257 on build GRCh38
Cytoband
14q32.33
Assay ID Hs03878165_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 113146

Gene Name:

 AHNAK nucleoprotein 2

Gene Aliases:

 C14orf78

Location:

 Chr.14:104937253-104978357 on Build GRCh38

Assay Gene Location:

 Within Exon 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
AHNAK2 NM_138420.2 7 14314 NP_612429.2
XM_005267299.1 7 14167 XP_005267356.1
AB095939.1 1 5215 BAC23115.1
AK126472.1 1 796
BC090889.1 AAH90889.1
BX537923.1 1 196 CAD97904.1
BX538040.1 CAD97981.1
BX538106.1 1 436 CAD98019.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv566099 Chr.14:104818822 - 104946204 on Build GRCh38 Gain CEP170B LINC00638 PLD4 AHNAK2
nsv566139 Chr.14:104880959 - 104950810 on Build GRCh38 Loss CEP170B PLD4 AHNAK2
nsv566141 Chr.14:104938047 - 105089059 on Build GRCh38 Gain GPR132 CDCA4 AHNAK2 C14orf79
nsv821194 Chr.14:104940674 - 104953760 on Build GRCh38 Deletion AHNAK2
dgv390n67 Chr.14:104941014 - 104953758 on Build GRCh38 Gain AHNAK2
esv25274 Chr.14:104934334 - 104953760 on Build GRCh38 Gain PLD4 AHNAK2
nsv1049253 Chr.14:104918622 - 105005518 on Build GRCh38 Gain PLD4 AHNAK2 C14orf79
nsv952276 Chr.14:104922864 - 105021963 on Build GRCh38 Deletion CDCA4 PLD4 AHNAK2 C14orf79
nsv1054574 Chr.14:103210111 - 105365114 on Build GRCh38 Loss ZFYVE21 LOC105370708 LINC00637 PPP1R13B LINC00638 ASPG LOC388022 MARK3 AHNAK2 CKB LOC107984648 LOC101929634 ZBTB42 TRMT61A MIR4710 C14orf180 EIF5 GPR132 MIR203A JAG2 PLD4 RD3L KLC1 MIR6765 LOC102723354 LOC105378183 XRCC3 BTBD6 APOPT1 ADSSL1 SIVA1 BAG5 TMEM179 CDCA4 C14orf2 KIF26A AKT1 TDRD9 CEP170B INF2 MIR203B LOC105370691 NUDT14 BRF1 LOC105370687 PACS2 SNORA28 C14orf79

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More Information


Additional Information:

For this assay, SNP(s) [rs76611205] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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