Canonical Allele Identifier: CA388675116
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875660A>T , CM000675.2:g.102875660A>T GRCh38
NC_000013.10:g.103528010A>T , CM000675.1:g.103528010A>T GRCh37
NC_000013.9:g.102326011A>T NCBI36
NG_007146.1:g.34837A>T , LRG_464:g.34837A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682632.1:n.4419A>T (ERCC5)
ENST00000682869.1:n.3967A>T (ERCC5)
ENST00000683246.1:n.4955A>T (ERCC5)
ENST00000683642.1:n.3548A>T (ERCC5)
ENST00000639132.1:c.3993A>T (BIVM-ERCC5) ENSP00000492684.1:p.Glu1331Asp
ENST00000639435.1:c.4680A>T (BIVM-ERCC5) ENSP00000491742.1:p.Glu1560Asp
ENST00000651002.1:c.*3079A>T (ERCC5) ENSP00000498809.1:n.*3079A>T
ENST00000651055.1:n.3445A>T (ERCC5)
ENST00000651281.1:n.3686A>T (ERCC5)
ENST00000651387.1:n.2802A>T (ERCC5)
ENST00000651470.1:c.*490A>T (ERCC5) ENSP00000498701.1:n.*490A>T
ENST00000652225.2:c.3318A>T (ERCC5) MANE Select ENSP00000498881.2:p.Glu1106Asp
ENST00000652613.1:c.2814A>T (ERCC5) ENSP00000498357.1:p.Glu938Asp
ENST00000355739.8:c.3318A>T (ERCC5) ENSP00000347978.4:p.Glu1106Asp
ENST00000375954.1:c.1017A>T (ERCC5) ENSP00000365121.1:p.Glu339Asp
ENST00000472247.1:n.478A>T (ERCC5)
ENST00000610537.4:c.3315A>T (ERCC5) ENSP00000478667.1:p.Glu1105Asp
NM_000123.3:c.3318A>T , LRG_464t1:c.3318A>T (ERCC5) NP_000114.2:p.Glu1106Asp
NM_001204425.1:c.4680A>T (BIVM-ERCC5) NP_001191354.1:p.Glu1560Asp
NM_000123.4:c.3318A>T (ERCC5) MANE Select NP_000114.3:p.Glu1106Asp
NM_001204425.2:c.4680A>T (BIVM-ERCC5) NP_001191354.2:p.Glu1560Asp