Genomic Map
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Target Gene Details
Entrez Gene ID: | 1113 |
Gene Name: | chromogranin A |
Gene Aliases: |
CGA |
Location: |
Chr.14:92922589-92935293 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CHGA | NM_001275.3 | NP_001266.1 | ||
| NM_001301690.1 | NP_001288619.1 | |||
| XM_011536370.1 | XP_011534672.1 | |||
| BC001059.2 | AAH01059.1 | |||
| BC006459.1 | AAH06459.1 | |||
| BC009384.2 | AAH09384.2 | |||
| BC012755.2 | AAH12755.2 | |||
| J03483.1 | AAA52017.1 | |||
| J03915.1 | AAA52018.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3892576 | Chr.14:92932504 - 92938764 on Build GRCh38 | Loss |
 ITPK1
CHGA
|
| nsv1400 | Chr.14:92928206 - 92973049 on Build GRCh38 | Deletion |
ITPK1
CHGA
|
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Additional Information:
For this assay, SNP(s) [rs141846973] 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
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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