Canonical Allele Identifier: CA388674919

Gene: ERCC5 BIVM-ERCC5

Linked Data

• gnomAD v4: 13-102875566-T-A
• MyVariant Identifiers: chr13:g.103527916T>A (hg19) ; chr13:g.102875566T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875566T>A , CM000675.2:g.102875566T>A	GRCh38
NC_000013.10:g.103527916T>A , CM000675.1:g.103527916T>A	GRCh37
NC_000013.9:g.102325917T>A	NCBI36
NG_007146.1:g.34743T>A , LRG_464:g.34743T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682632.1:n.4325T>A (ERCC5)
ENST00000682869.1:n.3873T>A (ERCC5)
ENST00000683246.1:n.4861T>A (ERCC5)
ENST00000683642.1:n.3454T>A (ERCC5)
ENST00000639132.1:c.3899T>A (BIVM-ERCC5)	ENSP00000492684.1:p.Leu1300His
ENST00000639435.1:c.4586T>A (BIVM-ERCC5)	ENSP00000491742.1:p.Leu1529His
ENST00000651002.1:c.*2985T>A (ERCC5)	ENSP00000498809.1:n.*2985T>A
ENST00000651055.1:n.3351T>A (ERCC5)
ENST00000651281.1:n.3592T>A (ERCC5)
ENST00000651387.1:n.2708T>A (ERCC5)
ENST00000651470.1:c.*396T>A (ERCC5)	ENSP00000498701.1:n.*396T>A
ENST00000652225.2:c.3224T>A (ERCC5) MANE Select	ENSP00000498881.2:p.Leu1075His
ENST00000652613.1:c.2720T>A (ERCC5)	ENSP00000498357.1:p.Leu907His
ENST00000355739.8:c.3224T>A (ERCC5)	ENSP00000347978.4:p.Leu1075His
ENST00000375954.1:c.923T>A (ERCC5)	ENSP00000365121.1:p.Leu308His
ENST00000472247.1:n.384T>A (ERCC5)
ENST00000610537.4:c.3221T>A (ERCC5)	ENSP00000478667.1:p.Leu1074His
NM_000123.3:c.3224T>A , LRG_464t1:c.3224T>A (ERCC5)	NP_000114.2:p.Leu1075His
NM_001204425.1:c.4586T>A (BIVM-ERCC5)	NP_001191354.1:p.Leu1529His
NM_000123.4:c.3224T>A (ERCC5) MANE Select	NP_000114.3:p.Leu1075His
NM_001204425.2:c.4586T>A (BIVM-ERCC5)	NP_001191354.2:p.Leu1529His