Canonical Allele Identifier: CA2115213202

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102868199G= , CM000675.2:g.102868199G=	GRCh38
NC_000013.10:g.103520549G= , CM000675.1:g.103520549G=	GRCh37
NC_000013.9:g.102318550G=	NCBI36
NG_007146.1:g.27376G= , LRG_464:g.27376G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000123.4:c.2620G= (ERCC5) MANE Select	NP_000114.3:p.Ala874=
ENST00000652225.2:c.2620G= (ERCC5) MANE Select	ENSP00000498881.2:p.Ala874=
NM_000123.3:c.2620G= , LRG_464t1:c.2620G= (ERCC5)	NP_000114.2:p.Ala874=
NM_001204425.1:c.3982G= (BIVM-ERCC5)	NP_001191354.1:p.Ala1328=
NM_001204425.2:c.3982G= (BIVM-ERCC5)	NP_001191354.2:p.Ala1328=
ENST00000355739.8:c.2620G= (ERCC5)	ENSP00000347978.4:p.Ala874=
ENST00000375954.1:c.319G= (ERCC5)	ENSP00000365121.1:p.Ala107=
ENST00000481099.1:n.740G= (ERCC5)
ENST00000602836.1:c.3896G= (BIVM-ERCC5)
ENST00000610537.4:c.2617G= (ERCC5)	ENSP00000478667.1:p.Ala873=
ENST00000639132.1:c.3295G= (BIVM-ERCC5)	ENSP00000492684.1:p.Ala1099=
ENST00000639435.1:c.3982G= (BIVM-ERCC5)	ENSP00000491742.1:p.Ala1328=
ENST00000651002.1:c.*2381G= (ERCC5)	ENSP00000498809.1:n.*2381G=
ENST00000651055.1:n.2749G= (ERCC5)
ENST00000651281.1:n.2988G= (ERCC5)
ENST00000651387.1:n.2104G= (ERCC5)
ENST00000651470.1:c.2620G= (ERCC5)	ENSP00000498701.1:p.Ala874=
ENST00000652613.1:c.2116G= (ERCC5)	ENSP00000498357.1:p.Ala706=
ENST00000682632.1:n.2861G= (ERCC5)
ENST00000682869.1:n.3269G= (ERCC5)
ENST00000683246.1:n.3397G= (ERCC5)