Canonical Allele Identifier: CA388674973
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875592T>C , CM000675.2:g.102875592T>C GRCh38
NC_000013.10:g.103527942T>C , CM000675.1:g.103527942T>C GRCh37
NC_000013.9:g.102325943T>C NCBI36
NG_007146.1:g.34769T>C , LRG_464:g.34769T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4351T>C (ERCC5)
ENST00000682869.1:n.3899T>C (ERCC5)
ENST00000683246.1:n.4887T>C (ERCC5)
ENST00000683642.1:n.3480T>C (ERCC5)
ENST00000639132.1:c.3925T>C (BIVM-ERCC5) ENSP00000492684.1:p.Cys1309Arg
ENST00000639435.1:c.4612T>C (BIVM-ERCC5) ENSP00000491742.1:p.Cys1538Arg
ENST00000651002.1:c.*3011T>C (ERCC5) ENSP00000498809.1:n.*3011T>C
ENST00000651055.1:n.3377T>C (ERCC5)
ENST00000651281.1:n.3618T>C (ERCC5)
ENST00000651387.1:n.2734T>C (ERCC5)
ENST00000651470.1:c.*422T>C (ERCC5) ENSP00000498701.1:n.*422T>C
ENST00000652225.2:c.3250T>C (ERCC5) MANE Select ENSP00000498881.2:p.Cys1084Arg
ENST00000652613.1:c.2746T>C (ERCC5) ENSP00000498357.1:p.Cys916Arg
ENST00000355739.8:c.3250T>C (ERCC5) ENSP00000347978.4:p.Cys1084Arg
ENST00000375954.1:c.949T>C (ERCC5) ENSP00000365121.1:p.Cys317Arg
ENST00000472247.1:n.410T>C (ERCC5)
ENST00000610537.4:c.3247T>C (ERCC5) ENSP00000478667.1:p.Cys1083Arg
NM_000123.3:c.3250T>C , LRG_464t1:c.3250T>C (ERCC5) NP_000114.2:p.Cys1084Arg
NM_001204425.1:c.4612T>C (BIVM-ERCC5) NP_001191354.1:p.Cys1538Arg
NM_000123.4:c.3250T>C (ERCC5) MANE Select NP_000114.3:p.Cys1084Arg
NM_001204425.2:c.4612T>C (BIVM-ERCC5) NP_001191354.2:p.Cys1538Arg