Canonical Allele Identifier: CA388569368
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856104G>T , CM000675.2:g.102856104G>T GRCh38
NC_000013.10:g.103508454G>T , CM000675.1:g.103508454G>T GRCh37
NC_000013.9:g.102306455G>T NCBI36
NG_007146.1:g.15281G>T , LRG_464:g.15281G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.761G>T (ERCC5)
ENST00000682869.1:n.1169G>T (ERCC5)
ENST00000683246.1:n.1297G>T (ERCC5)
ENST00000684184.1:n.1166G>T (ERCC5)
ENST00000639132.1:c.1195G>T (BIVM-ERCC5) ENSP00000492684.1:p.Ala399Ser
ENST00000639435.1:c.1882G>T (BIVM-ERCC5) ENSP00000491742.1:p.Ala628Ser
ENST00000651002.1:c.*281G>T (ERCC5) ENSP00000498809.1:n.*281G>T
ENST00000651055.1:n.649G>T (ERCC5)
ENST00000651281.1:n.888G>T (ERCC5)
ENST00000651470.1:c.520G>T (ERCC5) ENSP00000498701.1:p.Ala174Ser
ENST00000652225.2:c.520G>T (ERCC5) MANE Select ENSP00000498881.2:p.Ala174Ser
ENST00000652613.1:c.16G>T (ERCC5) ENSP00000498357.1:p.Ala6Ser
ENST00000355739.8:c.520G>T (ERCC5) ENSP00000347978.4:p.Ala174Ser
ENST00000535557.5:c.520G>T (ERCC5) ENSP00000442117.1:p.Ala174Ser
ENST00000602836.1:c.1796G>T (BIVM-ERCC5)
ENST00000610537.4:c.520G>T (ERCC5) ENSP00000478667.1:p.Ala174Ser
NM_000123.3:c.520G>T , LRG_464t1:c.520G>T (ERCC5) NP_000114.2:p.Ala174Ser
NM_001204425.1:c.1882G>T (BIVM-ERCC5) NP_001191354.1:p.Ala628Ser
NM_000123.4:c.520G>T (ERCC5) MANE Select NP_000114.3:p.Ala174Ser
NM_001204425.2:c.1882G>T (BIVM-ERCC5) NP_001191354.2:p.Ala628Ser