Canonical Allele Identifier: CA388675054
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102875632C>A , CM000675.2:g.102875632C>A GRCh38
NC_000013.10:g.103527982C>A , CM000675.1:g.103527982C>A GRCh37
NC_000013.9:g.102325983C>A NCBI36
NG_007146.1:g.34809C>A , LRG_464:g.34809C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.4391C>A (ERCC5)
ENST00000682869.1:n.3939C>A (ERCC5)
ENST00000683246.1:n.4927C>A (ERCC5)
ENST00000683642.1:n.3520C>A (ERCC5)
ENST00000639132.1:c.3965C>A (BIVM-ERCC5) ENSP00000492684.1:p.Ser1322Tyr
ENST00000639435.1:c.4652C>A (BIVM-ERCC5) ENSP00000491742.1:p.Ser1551Tyr
ENST00000651002.1:c.*3051C>A (ERCC5) ENSP00000498809.1:n.*3051C>A
ENST00000651055.1:n.3417C>A (ERCC5)
ENST00000651281.1:n.3658C>A (ERCC5)
ENST00000651387.1:n.2774C>A (ERCC5)
ENST00000651470.1:c.*462C>A (ERCC5) ENSP00000498701.1:n.*462C>A
ENST00000652225.2:c.3290C>A (ERCC5) MANE Select ENSP00000498881.2:p.Ser1097Tyr
ENST00000652613.1:c.2786C>A (ERCC5) ENSP00000498357.1:p.Ser929Tyr
ENST00000355739.8:c.3290C>A (ERCC5) ENSP00000347978.4:p.Ser1097Tyr
ENST00000375954.1:c.989C>A (ERCC5) ENSP00000365121.1:p.Ser330Tyr
ENST00000472247.1:n.450C>A (ERCC5)
ENST00000610537.4:c.3287C>A (ERCC5) ENSP00000478667.1:p.Ser1096Tyr
NM_000123.3:c.3290C>A , LRG_464t1:c.3290C>A (ERCC5) NP_000114.2:p.Ser1097Tyr
NM_001204425.1:c.4652C>A (BIVM-ERCC5) NP_001191354.1:p.Ser1551Tyr
NM_000123.4:c.3290C>A (ERCC5) MANE Select NP_000114.3:p.Ser1097Tyr
NM_001204425.2:c.4652C>A (BIVM-ERCC5) NP_001191354.2:p.Ser1551Tyr