Canonical Allele Identifier: CA388673521

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103525646A>T (hg19) ; chr13:g.102873296A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873296A>T , CM000675.2:g.102873296A>T	GRCh38
NC_000013.10:g.103525646A>T , CM000675.1:g.103525646A>T	GRCh37
NC_000013.9:g.102323647A>T	NCBI36
NG_007146.1:g.32473A>T , LRG_464:g.32473A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.4018A>T (ERCC5)
ENST00000682869.1:n.3566A>T (ERCC5)
ENST00000683246.1:n.4554A>T (ERCC5)
ENST00000683642.1:n.3147A>T (ERCC5)
ENST00000639132.1:c.3592A>T (BIVM-ERCC5)	ENSP00000492684.1:p.Thr1198Ser
ENST00000639435.1:c.4279A>T (BIVM-ERCC5)	ENSP00000491742.1:p.Thr1427Ser
ENST00000651002.1:c.*2678A>T (ERCC5)	ENSP00000498809.1:n.*2678A>T
ENST00000651055.1:n.3044A>T (ERCC5)
ENST00000651281.1:n.3285A>T (ERCC5)
ENST00000651387.1:n.2401A>T (ERCC5)
ENST00000651470.1:c.*89A>T (ERCC5)	ENSP00000498701.1:n.*89A>T
ENST00000652225.2:c.2917A>T (ERCC5) MANE Select	ENSP00000498881.2:p.Thr973Ser
ENST00000652613.1:c.2413A>T (ERCC5)	ENSP00000498357.1:p.Thr805Ser
ENST00000355739.8:c.2917A>T (ERCC5)	ENSP00000347978.4:p.Thr973Ser
ENST00000375954.1:c.616A>T (ERCC5)	ENSP00000365121.1:p.Thr206Ser
ENST00000610537.4:c.2914A>T (ERCC5)	ENSP00000478667.1:p.Thr972Ser
NM_000123.3:c.2917A>T , LRG_464t1:c.2917A>T (ERCC5)	NP_000114.2:p.Thr973Ser
NM_001204425.1:c.4279A>T (BIVM-ERCC5)	NP_001191354.1:p.Thr1427Ser
NM_000123.4:c.2917A>T (ERCC5) MANE Select	NP_000114.3:p.Thr973Ser
NM_001204425.2:c.4279A>T (BIVM-ERCC5)	NP_001191354.2:p.Thr1427Ser