Canonical Allele Identifier: CA2115215335

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873284A= , CM000675.2:g.102873284A=	GRCh38
NC_000013.10:g.103525634A= , CM000675.1:g.103525634A=	GRCh37
NC_000013.9:g.102323635A=	NCBI36
NG_007146.1:g.32461A= , LRG_464:g.32461A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4006A= (ERCC5)
ENST00000682869.1:n.3554A= (ERCC5)
ENST00000683246.1:n.4542A= (ERCC5)
ENST00000683642.1:n.3135A= (ERCC5)
ENST00000639132.1:c.3580A= (BIVM-ERCC5)	ENSP00000492684.1:p.Asn1194=
ENST00000639435.1:c.4267A= (BIVM-ERCC5)	ENSP00000491742.1:p.Asn1423=
ENST00000651002.1:c.*2666A= (ERCC5)	ENSP00000498809.1:n.*2666A=
ENST00000651055.1:n.3032A= (ERCC5)
ENST00000651281.1:n.3273A= (ERCC5)
ENST00000651387.1:n.2389A= (ERCC5)
ENST00000651470.1:c.*77A= (ERCC5)	ENSP00000498701.1:n.*77A=
ENST00000652225.2:c.2905A= (ERCC5) MANE Select	ENSP00000498881.2:p.Asn969=
ENST00000652613.1:c.2401A= (ERCC5)	ENSP00000498357.1:p.Asn801=
ENST00000355739.8:c.2905A= (ERCC5)	ENSP00000347978.4:p.Asn969=
ENST00000375954.1:c.604A= (ERCC5)	ENSP00000365121.1:p.Asn202=
ENST00000610537.4:c.2902A= (ERCC5)	ENSP00000478667.1:p.Asn968=
NM_000123.3:c.2905A= , LRG_464t1:c.2905A= (ERCC5)	NP_000114.2:p.Asn969=
NM_001204425.1:c.4267A= (BIVM-ERCC5)	NP_001191354.1:p.Asn1423=
NM_000123.4:c.2905A= (ERCC5) MANE Select	NP_000114.3:p.Asn969=
NM_001204425.2:c.4267A= (BIVM-ERCC5)	NP_001191354.2:p.Asn1423=