Canonical Allele Identifier: CA388569344
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856095C>G , CM000675.2:g.102856095C>G GRCh38
NC_000013.10:g.103508445C>G , CM000675.1:g.103508445C>G GRCh37
NC_000013.9:g.102306446C>G NCBI36
NG_007146.1:g.15272C>G , LRG_464:g.15272C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.752C>G (ERCC5)
ENST00000682869.1:n.1160C>G (ERCC5)
ENST00000683246.1:n.1288C>G (ERCC5)
ENST00000684184.1:n.1157C>G (ERCC5)
ENST00000638434.1:c.609C>G (BIVM-ERCC5)
ENST00000639132.1:c.1186C>G (BIVM-ERCC5) ENSP00000492684.1:p.Gln396Glu
ENST00000639435.1:c.1873C>G (BIVM-ERCC5) ENSP00000491742.1:p.Gln625Glu
ENST00000651002.1:c.*272C>G (ERCC5) ENSP00000498809.1:n.*272C>G
ENST00000651055.1:n.640C>G (ERCC5)
ENST00000651281.1:n.879C>G (ERCC5)
ENST00000651470.1:c.511C>G (ERCC5) ENSP00000498701.1:p.Gln171Glu
ENST00000652225.2:c.511C>G (ERCC5) MANE Select ENSP00000498881.2:p.Gln171Glu
ENST00000652613.1:c.7C>G (ERCC5) ENSP00000498357.1:p.Gln3Glu
ENST00000355739.8:c.511C>G (ERCC5) ENSP00000347978.4:p.Gln171Glu
ENST00000535557.5:c.511C>G (ERCC5) ENSP00000442117.1:p.Gln171Glu
ENST00000602836.1:c.1787C>G (BIVM-ERCC5)
ENST00000610537.4:c.511C>G (ERCC5) ENSP00000478667.1:p.Gln171Glu
NM_000123.3:c.511C>G , LRG_464t1:c.511C>G (ERCC5) NP_000114.2:p.Gln171Glu
NM_001204425.1:c.1873C>G (BIVM-ERCC5) NP_001191354.1:p.Gln625Glu
NM_000123.4:c.511C>G (ERCC5) MANE Select NP_000114.3:p.Gln171Glu
NM_001204425.2:c.1873C>G (BIVM-ERCC5) NP_001191354.2:p.Gln625Glu