Canonical Allele Identifier: CA2729197895
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

dbSNP Id: rs2140520976

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856044A>T , CM000675.2:g.102856044A>T GRCh38
NC_000013.10:g.103508394A>T , CM000675.1:g.103508394A>T GRCh37
NC_000013.9:g.102306395A>T NCBI36
NG_007146.1:g.15221A>T , LRG_464:g.15221A>T

Transcript Alleles

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