Canonical Allele Identifier: CA388673514
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102873294A>C , CM000675.2:g.102873294A>C GRCh38
NC_000013.10:g.103525644A>C , CM000675.1:g.103525644A>C GRCh37
NC_000013.9:g.102323645A>C NCBI36
NG_007146.1:g.32471A>C , LRG_464:g.32471A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4016A>C (ERCC5)
ENST00000682869.1:n.3564A>C (ERCC5)
ENST00000683246.1:n.4552A>C (ERCC5)
ENST00000683642.1:n.3145A>C (ERCC5)
ENST00000639132.1:c.3590A>C (BIVM-ERCC5) ENSP00000492684.1:p.Lys1197Thr
ENST00000639435.1:c.4277A>C (BIVM-ERCC5) ENSP00000491742.1:p.Lys1426Thr
ENST00000651002.1:c.*2676A>C (ERCC5) ENSP00000498809.1:n.*2676A>C
ENST00000651055.1:n.3042A>C (ERCC5)
ENST00000651281.1:n.3283A>C (ERCC5)
ENST00000651387.1:n.2399A>C (ERCC5)
ENST00000651470.1:c.*87A>C (ERCC5) ENSP00000498701.1:n.*87A>C
ENST00000652225.2:c.2915A>C (ERCC5) MANE Select ENSP00000498881.2:p.Lys972Thr
ENST00000652613.1:c.2411A>C (ERCC5) ENSP00000498357.1:p.Lys804Thr
ENST00000355739.8:c.2915A>C (ERCC5) ENSP00000347978.4:p.Lys972Thr
ENST00000375954.1:c.614A>C (ERCC5) ENSP00000365121.1:p.Lys205Thr
ENST00000610537.4:c.2912A>C (ERCC5) ENSP00000478667.1:p.Lys971Thr
NM_000123.3:c.2915A>C , LRG_464t1:c.2915A>C (ERCC5) NP_000114.2:p.Lys972Thr
NM_001204425.1:c.4277A>C (BIVM-ERCC5) NP_001191354.1:p.Lys1426Thr
NM_000123.4:c.2915A>C (ERCC5) MANE Select NP_000114.3:p.Lys972Thr
NM_001204425.2:c.4277A>C (BIVM-ERCC5) NP_001191354.2:p.Lys1426Thr