Canonical Allele Identifier: CA388674977
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs372662617

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875594C>G , CM000675.2:g.102875594C>G GRCh38
NC_000013.10:g.103527944C>G , CM000675.1:g.103527944C>G GRCh37
NC_000013.9:g.102325945C>G NCBI36
NG_007146.1:g.34771C>G , LRG_464:g.34771C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4353C>G (ERCC5)
ENST00000682869.1:n.3901C>G (ERCC5)
ENST00000683246.1:n.4889C>G (ERCC5)
ENST00000683642.1:n.3482C>G (ERCC5)
ENST00000639132.1:c.3927C>G (BIVM-ERCC5) ENSP00000492684.1:p.Cys1309Trp
ENST00000639435.1:c.4614C>G (BIVM-ERCC5) ENSP00000491742.1:p.Cys1538Trp
ENST00000651002.1:c.*3013C>G (ERCC5) ENSP00000498809.1:n.*3013C>G
ENST00000651055.1:n.3379C>G (ERCC5)
ENST00000651281.1:n.3620C>G (ERCC5)
ENST00000651387.1:n.2736C>G (ERCC5)
ENST00000651470.1:c.*424C>G (ERCC5) ENSP00000498701.1:n.*424C>G
ENST00000652225.2:c.3252C>G (ERCC5) MANE Select ENSP00000498881.2:p.Cys1084Trp
ENST00000652613.1:c.2748C>G (ERCC5) ENSP00000498357.1:p.Cys916Trp
ENST00000355739.8:c.3252C>G (ERCC5) ENSP00000347978.4:p.Cys1084Trp
ENST00000375954.1:c.951C>G (ERCC5) ENSP00000365121.1:p.Cys317Trp
ENST00000472247.1:n.412C>G (ERCC5)
ENST00000610537.4:c.3249C>G (ERCC5) ENSP00000478667.1:p.Cys1083Trp
NM_000123.3:c.3252C>G , LRG_464t1:c.3252C>G (ERCC5) NP_000114.2:p.Cys1084Trp
NM_001204425.1:c.4614C>G (BIVM-ERCC5) NP_001191354.1:p.Cys1538Trp
NM_000123.4:c.3252C>G (ERCC5) MANE Select NP_000114.3:p.Cys1084Trp
NM_001204425.2:c.4614C>G (BIVM-ERCC5) NP_001191354.2:p.Cys1538Trp