Canonical Allele Identifier: CA2115215356

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873337C= , CM000675.2:g.102873337C=	GRCh38
NC_000013.10:g.103525687C= , CM000675.1:g.103525687C=	GRCh37
NC_000013.9:g.102323688C=	NCBI36
NG_007146.1:g.32514C= , LRG_464:g.32514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4059C= (ERCC5)
ENST00000682869.1:n.3607C= (ERCC5)
ENST00000683246.1:n.4595C= (ERCC5)
ENST00000683642.1:n.3188C= (ERCC5)
ENST00000639132.1:c.3633C= (BIVM-ERCC5)	ENSP00000492684.1:p.Ala1211=
ENST00000639435.1:c.4320C= (BIVM-ERCC5)	ENSP00000491742.1:p.Ala1440=
ENST00000651002.1:c.*2719C= (ERCC5)	ENSP00000498809.1:n.*2719C=
ENST00000651055.1:n.3085C= (ERCC5)
ENST00000651281.1:n.3326C= (ERCC5)
ENST00000651387.1:n.2442C= (ERCC5)
ENST00000651470.1:c.*130C= (ERCC5)	ENSP00000498701.1:n.*130C=
ENST00000652225.2:c.2958C= (ERCC5) MANE Select	ENSP00000498881.2:p.Ala986=
ENST00000652613.1:c.2454C= (ERCC5)	ENSP00000498357.1:p.Ala818=
ENST00000355739.8:c.2958C= (ERCC5)	ENSP00000347978.4:p.Ala986=
ENST00000375954.1:c.657C= (ERCC5)	ENSP00000365121.1:p.Ala219=
ENST00000610537.4:c.2955C= (ERCC5)	ENSP00000478667.1:p.Ala985=
NM_000123.3:c.2958C= , LRG_464t1:c.2958C= (ERCC5)	NP_000114.2:p.Ala986=
NM_001204425.1:c.4320C= (BIVM-ERCC5)	NP_001191354.1:p.Ala1440=
NM_000123.4:c.2958C= (ERCC5) MANE Select	NP_000114.3:p.Ala986=
NM_001204425.2:c.4320C= (BIVM-ERCC5)	NP_001191354.2:p.Ala1440=