Canonical Allele Identifier: CA388569259
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856062G>C , CM000675.2:g.102856062G>C GRCh38
NC_000013.10:g.103508412G>C , CM000675.1:g.103508412G>C GRCh37
NC_000013.9:g.102306413G>C NCBI36
NG_007146.1:g.15239G>C , LRG_464:g.15239G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.719G>C (ERCC5)
ENST00000682869.1:n.1127G>C (ERCC5)
ENST00000683246.1:n.1255G>C (ERCC5)
ENST00000684184.1:n.1124G>C (ERCC5)
ENST00000638434.1:c.576G>C (BIVM-ERCC5)
ENST00000639132.1:c.1153G>C (BIVM-ERCC5) ENSP00000492684.1:p.Glu385Gln
ENST00000639435.1:c.1840G>C (BIVM-ERCC5) ENSP00000491742.1:p.Glu614Gln
ENST00000651002.1:c.*239G>C (ERCC5) ENSP00000498809.1:n.*239G>C
ENST00000651055.1:n.607G>C (ERCC5)
ENST00000651281.1:n.846G>C (ERCC5)
ENST00000651470.1:c.478G>C (ERCC5) ENSP00000498701.1:p.Glu160Gln
ENST00000652225.2:c.478G>C (ERCC5) MANE Select ENSP00000498881.2:p.Glu160Gln
ENST00000652613.1:c.-27G>C (ERCC5) ENSP00000498357.1:n.-27G>C
ENST00000355739.8:c.478G>C (ERCC5) ENSP00000347978.4:p.Glu160Gln
ENST00000535557.5:c.478G>C (ERCC5) ENSP00000442117.1:p.Glu160Gln
ENST00000602836.1:c.1754G>C (BIVM-ERCC5)
ENST00000610537.4:c.478G>C (ERCC5) ENSP00000478667.1:p.Glu160Gln
NM_000123.3:c.478G>C , LRG_464t1:c.478G>C (ERCC5) NP_000114.2:p.Glu160Gln
NM_001204425.1:c.1840G>C (BIVM-ERCC5) NP_001191354.1:p.Glu614Gln
NM_000123.4:c.478G>C (ERCC5) MANE Select NP_000114.3:p.Glu160Gln
NM_001204425.2:c.1840G>C (BIVM-ERCC5) NP_001191354.2:p.Glu614Gln