Canonical Allele Identifier: CA2115216480
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875588T= , CM000675.2:g.102875588T= GRCh38
NC_000013.10:g.103527938T= , CM000675.1:g.103527938T= GRCh37
NC_000013.9:g.102325939T= NCBI36
NG_007146.1:g.34765T= , LRG_464:g.34765T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4347T= (ERCC5)
ENST00000682869.1:n.3895T= (ERCC5)
ENST00000683246.1:n.4883T= (ERCC5)
ENST00000683642.1:n.3476T= (ERCC5)
ENST00000639132.1:c.3921T= (BIVM-ERCC5) ENSP00000492684.1:p.Asn1307=
ENST00000639435.1:c.4608T= (BIVM-ERCC5) ENSP00000491742.1:p.Asn1536=
ENST00000651002.1:c.*3007T= (ERCC5) ENSP00000498809.1:n.*3007T=
ENST00000651055.1:n.3373T= (ERCC5)
ENST00000651281.1:n.3614T= (ERCC5)
ENST00000651387.1:n.2730T= (ERCC5)
ENST00000651470.1:c.*418T= (ERCC5) ENSP00000498701.1:n.*418T=
ENST00000652225.2:c.3246T= (ERCC5) MANE Select ENSP00000498881.2:p.Asn1082=
ENST00000652613.1:c.2742T= (ERCC5) ENSP00000498357.1:p.Asn914=
ENST00000355739.8:c.3246T= (ERCC5) ENSP00000347978.4:p.Asn1082=
ENST00000375954.1:c.945T= (ERCC5) ENSP00000365121.1:p.Asn315=
ENST00000472247.1:n.406T= (ERCC5)
ENST00000610537.4:c.3243T= (ERCC5) ENSP00000478667.1:p.Asn1081=
NM_000123.3:c.3246T= , LRG_464t1:c.3246T= (ERCC5) NP_000114.2:p.Asn1082=
NM_001204425.1:c.4608T= (BIVM-ERCC5) NP_001191354.1:p.Asn1536=
NM_000123.4:c.3246T= (ERCC5) MANE Select NP_000114.3:p.Asn1082=
NM_001204425.2:c.4608T= (BIVM-ERCC5) NP_001191354.2:p.Asn1536=