Canonical Allele Identifier: CA388569302

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103508428G>A (hg19) ; chr13:g.102856078G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102856078G>A , CM000675.2:g.102856078G>A	GRCh38
NC_000013.10:g.103508428G>A , CM000675.1:g.103508428G>A	GRCh37
NC_000013.9:g.102306429G>A	NCBI36
NG_007146.1:g.15255G>A , LRG_464:g.15255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.735G>A (ERCC5)
ENST00000682869.1:n.1143G>A (ERCC5)
ENST00000683246.1:n.1271G>A (ERCC5)
ENST00000684184.1:n.1140G>A (ERCC5)
ENST00000638434.1:c.592G>A (BIVM-ERCC5)
ENST00000639132.1:c.1169G>A (BIVM-ERCC5)	ENSP00000492684.1:p.Trp390Ter
ENST00000639435.1:c.1856G>A (BIVM-ERCC5)	ENSP00000491742.1:p.Trp619Ter
ENST00000651002.1:c.*255G>A (ERCC5)	ENSP00000498809.1:n.*255G>A
ENST00000651055.1:n.623G>A (ERCC5)
ENST00000651281.1:n.862G>A (ERCC5)
ENST00000651470.1:c.494G>A (ERCC5)	ENSP00000498701.1:p.Trp165Ter
ENST00000652225.2:c.494G>A (ERCC5) MANE Select	ENSP00000498881.2:p.Trp165Ter
ENST00000652613.1:c.-11G>A (ERCC5)	ENSP00000498357.1:n.-11G>A
ENST00000355739.8:c.494G>A (ERCC5)	ENSP00000347978.4:p.Trp165Ter
ENST00000535557.5:c.494G>A (ERCC5)	ENSP00000442117.1:p.Trp165Ter
ENST00000602836.1:c.1770G>A (BIVM-ERCC5)
ENST00000610537.4:c.494G>A (ERCC5)	ENSP00000478667.1:p.Trp165Ter
NM_000123.3:c.494G>A , LRG_464t1:c.494G>A (ERCC5)	NP_000114.2:p.Trp165Ter
NM_001204425.1:c.1856G>A (BIVM-ERCC5)	NP_001191354.1:p.Trp619Ter
NM_000123.4:c.494G>A (ERCC5) MANE Select	NP_000114.3:p.Trp165Ter
NM_001204425.2:c.1856G>A (BIVM-ERCC5)	NP_001191354.2:p.Trp619Ter