Canonical Allele Identifier: CA2115216516

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102875656C= , CM000675.2:g.102875656C=	GRCh38
NC_000013.10:g.103528006C= , CM000675.1:g.103528006C=	GRCh37
NC_000013.9:g.102326007C=	NCBI36
NG_007146.1:g.34833C= , LRG_464:g.34833C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682632.1:n.4415C= (ERCC5)
ENST00000682869.1:n.3963C= (ERCC5)
ENST00000683246.1:n.4951C= (ERCC5)
ENST00000683642.1:n.3544C= (ERCC5)
ENST00000639132.1:c.3989C= (BIVM-ERCC5)	ENSP00000492684.1:p.Ala1330=
ENST00000639435.1:c.4676C= (BIVM-ERCC5)	ENSP00000491742.1:p.Ala1559=
ENST00000651002.1:c.*3075C= (ERCC5)	ENSP00000498809.1:n.*3075C=
ENST00000651055.1:n.3441C= (ERCC5)
ENST00000651281.1:n.3682C= (ERCC5)
ENST00000651387.1:n.2798C= (ERCC5)
ENST00000651470.1:c.*486C= (ERCC5)	ENSP00000498701.1:n.*486C=
ENST00000652225.2:c.3314C= (ERCC5) MANE Select	ENSP00000498881.2:p.Ala1105=
ENST00000652613.1:c.2810C= (ERCC5)	ENSP00000498357.1:p.Ala937=
ENST00000355739.8:c.3314C= (ERCC5)	ENSP00000347978.4:p.Ala1105=
ENST00000375954.1:c.1013C= (ERCC5)	ENSP00000365121.1:p.Ala338=
ENST00000472247.1:n.474C= (ERCC5)
ENST00000610537.4:c.3311C= (ERCC5)	ENSP00000478667.1:p.Ala1104=
NM_000123.3:c.3314C= , LRG_464t1:c.3314C= (ERCC5)	NP_000114.2:p.Ala1105=
NM_001204425.1:c.4676C= (BIVM-ERCC5)	NP_001191354.1:p.Ala1559=
NM_000123.4:c.3314C= (ERCC5) MANE Select	NP_000114.3:p.Ala1105=
NM_001204425.2:c.4676C= (BIVM-ERCC5)	NP_001191354.2:p.Ala1559=