Canonical Allele Identifier: CA2115215339

Gene: ERCC5 BIVM-ERCC5

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873292G= , CM000675.2:g.102873292G=	GRCh38
NC_000013.10:g.103525642G= , CM000675.1:g.103525642G=	GRCh37
NC_000013.9:g.102323643G=	NCBI36
NG_007146.1:g.32469G= , LRG_464:g.32469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4014G= (ERCC5)
ENST00000682869.1:n.3562G= (ERCC5)
ENST00000683246.1:n.4550G= (ERCC5)
ENST00000683642.1:n.3143G= (ERCC5)
ENST00000639132.1:c.3588G= (BIVM-ERCC5)	ENSP00000492684.1:p.Thr1196=
ENST00000639435.1:c.4275G= (BIVM-ERCC5)	ENSP00000491742.1:p.Thr1425=
ENST00000651002.1:c.*2674G= (ERCC5)	ENSP00000498809.1:n.*2674G=
ENST00000651055.1:n.3040G= (ERCC5)
ENST00000651281.1:n.3281G= (ERCC5)
ENST00000651387.1:n.2397G= (ERCC5)
ENST00000651470.1:c.*85G= (ERCC5)	ENSP00000498701.1:n.*85G=
ENST00000652225.2:c.2913G= (ERCC5) MANE Select	ENSP00000498881.2:p.Thr971=
ENST00000652613.1:c.2409G= (ERCC5)	ENSP00000498357.1:p.Thr803=
ENST00000355739.8:c.2913G= (ERCC5)	ENSP00000347978.4:p.Thr971=
ENST00000375954.1:c.612G= (ERCC5)	ENSP00000365121.1:p.Thr204=
ENST00000610537.4:c.2910G= (ERCC5)	ENSP00000478667.1:p.Thr970=
NM_000123.3:c.2913G= , LRG_464t1:c.2913G= (ERCC5)	NP_000114.2:p.Thr971=
NM_001204425.1:c.4275G= (BIVM-ERCC5)	NP_001191354.1:p.Thr1425=
NM_000123.4:c.2913G= (ERCC5) MANE Select	NP_000114.3:p.Thr971=
NM_001204425.2:c.4275G= (BIVM-ERCC5)	NP_001191354.2:p.Thr1425=