Canonical Allele Identifier: CA388569309

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103508430C>T (hg19) ; chr13:g.102856080C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102856080C>T , CM000675.2:g.102856080C>T	GRCh38
NC_000013.10:g.103508430C>T , CM000675.1:g.103508430C>T	GRCh37
NC_000013.9:g.102306431C>T	NCBI36
NG_007146.1:g.15257C>T , LRG_464:g.15257C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.737C>T (ERCC5)
ENST00000682869.1:n.1145C>T (ERCC5)
ENST00000683246.1:n.1273C>T (ERCC5)
ENST00000684184.1:n.1142C>T (ERCC5)
ENST00000638434.1:c.594C>T (BIVM-ERCC5)
ENST00000639132.1:c.1171C>T (BIVM-ERCC5)	ENSP00000492684.1:p.Gln391Ter
ENST00000639435.1:c.1858C>T (BIVM-ERCC5)	ENSP00000491742.1:p.Gln620Ter
ENST00000651002.1:c.*257C>T (ERCC5)	ENSP00000498809.1:n.*257C>T
ENST00000651055.1:n.625C>T (ERCC5)
ENST00000651281.1:n.864C>T (ERCC5)
ENST00000651470.1:c.496C>T (ERCC5)	ENSP00000498701.1:p.Gln166Ter
ENST00000652225.2:c.496C>T (ERCC5) MANE Select	ENSP00000498881.2:p.Gln166Ter
ENST00000652613.1:c.-9C>T (ERCC5)	ENSP00000498357.1:n.-9C>T
ENST00000355739.8:c.496C>T (ERCC5)	ENSP00000347978.4:p.Gln166Ter
ENST00000535557.5:c.496C>T (ERCC5)	ENSP00000442117.1:p.Gln166Ter
ENST00000602836.1:c.1772C>T (BIVM-ERCC5)
ENST00000610537.4:c.496C>T (ERCC5)	ENSP00000478667.1:p.Gln166Ter
NM_000123.3:c.496C>T , LRG_464t1:c.496C>T (ERCC5)	NP_000114.2:p.Gln166Ter
NM_001204425.1:c.1858C>T (BIVM-ERCC5)	NP_001191354.1:p.Gln620Ter
NM_000123.4:c.496C>T (ERCC5) MANE Select	NP_000114.3:p.Gln166Ter
NM_001204425.2:c.1858C>T (BIVM-ERCC5)	NP_001191354.2:p.Gln620Ter