Canonical Allele Identifier: CA388574146

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs1196088675
• gnomAD v2: 13-103515241-T-G
• gnomAD v4: 13-102862891-T-G
• MyVariant Identifiers: chr13:g.103515241T>G (hg19) ; chr13:g.102862891T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862891T>G , CM000675.2:g.102862891T>G	GRCh38
NC_000013.10:g.103515241T>G , CM000675.1:g.103515241T>G	GRCh37
NC_000013.9:g.102313242T>G	NCBI36
NG_007146.1:g.22068T>G , LRG_464:g.22068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.1983T>G (ERCC5)
ENST00000682869.1:n.2391T>G (ERCC5)
ENST00000683246.1:n.2519T>G (ERCC5)
ENST00000639132.1:c.2417T>G (BIVM-ERCC5)	ENSP00000492684.1:p.Val806Gly
ENST00000639435.1:c.3104T>G (BIVM-ERCC5)	ENSP00000491742.1:p.Val1035Gly
ENST00000651002.1:c.*1503T>G (ERCC5)	ENSP00000498809.1:n.*1503T>G
ENST00000651055.1:n.1871T>G (ERCC5)
ENST00000651281.1:n.2110T>G (ERCC5)
ENST00000651387.1:n.1226T>G (ERCC5)
ENST00000651470.1:c.1742T>G (ERCC5)	ENSP00000498701.1:p.Val581Gly
ENST00000652225.2:c.1742T>G (ERCC5) MANE Select	ENSP00000498881.2:p.Val581Gly
ENST00000652613.1:c.1238T>G (ERCC5)	ENSP00000498357.1:p.Val413Gly
ENST00000355739.8:c.1742T>G (ERCC5)	ENSP00000347978.4:p.Val581Gly
ENST00000602836.1:c.3018T>G (BIVM-ERCC5)
ENST00000610537.4:c.1742T>G (ERCC5)	ENSP00000478667.1:p.Val581Gly
NM_000123.3:c.1742T>G , LRG_464t1:c.1742T>G (ERCC5)	NP_000114.2:p.Val581Gly
NM_001204425.1:c.3104T>G (BIVM-ERCC5)	NP_001191354.1:p.Val1035Gly
NM_000123.4:c.1742T>G (ERCC5) MANE Select	NP_000114.3:p.Val581Gly
NM_001204425.2:c.3104T>G (BIVM-ERCC5)	NP_001191354.2:p.Val1035Gly