Canonical Allele Identifier: CA2115207993
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1882404557

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856032A>T , CM000675.2:g.102856032A>T GRCh38
NC_000013.10:g.103508382A>T , CM000675.1:g.103508382A>T GRCh37
NC_000013.9:g.102306383A>T NCBI36
NG_007146.1:g.15209A>T , LRG_464:g.15209A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.709-20A>T (ERCC5)
ENST00000682869.1:n.1117-20A>T (ERCC5)
ENST00000683246.1:n.1245-20A>T (ERCC5)
ENST00000684184.1:n.1114-20A>T (ERCC5)
ENST00000638434.1:c.566-20A>T (BIVM-ERCC5)
ENST00000639132.1:c.1143-20A>T (BIVM-ERCC5) ENSP00000492684.1:n.1143-20A>T
ENST00000639435.1:c.1830-20A>T (BIVM-ERCC5) ENSP00000491742.1:n.1830-20A>T
ENST00000651002.1:c.*229-20A>T (ERCC5) ENSP00000498809.1:n.*229-20A>T
ENST00000651055.1:n.597-20A>T (ERCC5)
ENST00000651281.1:n.836-20A>T (ERCC5)
ENST00000651470.1:c.468-20A>T (ERCC5) ENSP00000498701.1:n.468-20A>T
ENST00000652225.2:c.468-20A>T (ERCC5) MANE Select ENSP00000498881.2:n.468-20A>T
ENST00000652613.1:c.-37-20A>T (ERCC5) ENSP00000498357.1:n.-37-20A>T
ENST00000355739.8:c.468-20A>T (ERCC5) ENSP00000347978.4:n.468-20A>T
ENST00000535557.5:c.468-20A>T (ERCC5) ENSP00000442117.1:n.468-20A>T
ENST00000602836.1:c.1744-20A>T (BIVM-ERCC5)
ENST00000610537.4:c.468-20A>T (ERCC5) ENSP00000478667.1:n.468-20A>T
NM_000123.3:c.468-20A>T , LRG_464t1:c.468-20A>T (ERCC5) NP_000114.2:n.468-20A>T
NM_001204425.1:c.1830-20A>T (BIVM-ERCC5) NP_001191354.1:n.1830-20A>T
NM_000123.4:c.468-20A>T (ERCC5) MANE Select NP_000114.3:n.468-20A>T
NM_001204425.2:c.1830-20A>T (BIVM-ERCC5) NP_001191354.2:n.1830-20A>T