Canonical Allele Identifier: CA484968535
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.103515242C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102862892C>T , CM000675.2:g.102862892C>T GRCh38
NC_000013.10:g.103515242C>T , CM000675.1:g.103515242C>T GRCh37
NC_000013.9:g.102313243C>T NCBI36
NG_007146.1:g.22069C>T , LRG_464:g.22069C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.1984C>T (ERCC5)
ENST00000682869.1:n.2392C>T (ERCC5)
ENST00000683246.1:n.2520C>T (ERCC5)
ENST00000639132.1:c.2418C>T (BIVM-ERCC5) ENSP00000492684.1:p.Val806=
ENST00000639435.1:c.3105C>T (BIVM-ERCC5) ENSP00000491742.1:p.Val1035=
ENST00000651002.1:c.*1504C>T (ERCC5) ENSP00000498809.1:n.*1504C>T
ENST00000651055.1:n.1872C>T (ERCC5)
ENST00000651281.1:n.2111C>T (ERCC5)
ENST00000651387.1:n.1227C>T (ERCC5)
ENST00000651470.1:c.1743C>T (ERCC5) ENSP00000498701.1:p.Val581=
ENST00000652225.2:c.1743C>T (ERCC5) MANE Select ENSP00000498881.2:p.Val581=
ENST00000652613.1:c.1239C>T (ERCC5) ENSP00000498357.1:p.Val413=
ENST00000355739.8:c.1743C>T (ERCC5) ENSP00000347978.4:p.Val581=
ENST00000602836.1:c.3019C>T (BIVM-ERCC5)
ENST00000610537.4:c.1743C>T (ERCC5) ENSP00000478667.1:p.Val581=
NM_000123.3:c.1743C>T , LRG_464t1:c.1743C>T (ERCC5) NP_000114.2:p.Val581=
NM_001204425.1:c.3105C>T (BIVM-ERCC5) NP_001191354.1:p.Val1035=
NM_000123.4:c.1743C>T (ERCC5) MANE Select NP_000114.3:p.Val581=
NM_001204425.2:c.3105C>T (BIVM-ERCC5) NP_001191354.2:p.Val1035=