Canonical Allele Identifier: CA484968455

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103515206T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862856T>C , CM000675.2:g.102862856T>C	GRCh38
NC_000013.10:g.103515206T>C , CM000675.1:g.103515206T>C	GRCh37
NC_000013.9:g.102313207T>C	NCBI36
NG_007146.1:g.22033T>C , LRG_464:g.22033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.1948T>C (ERCC5)
ENST00000682869.1:n.2356T>C (ERCC5)
ENST00000683246.1:n.2484T>C (ERCC5)
ENST00000639132.1:c.2382T>C (BIVM-ERCC5)	ENSP00000492684.1:p.Cys794=
ENST00000639435.1:c.3069T>C (BIVM-ERCC5)	ENSP00000491742.1:p.Cys1023=
ENST00000651002.1:c.*1468T>C (ERCC5)	ENSP00000498809.1:n.*1468T>C
ENST00000651055.1:n.1836T>C (ERCC5)
ENST00000651281.1:n.2075T>C (ERCC5)
ENST00000651387.1:n.1191T>C (ERCC5)
ENST00000651470.1:c.1707T>C (ERCC5)	ENSP00000498701.1:p.Cys569=
ENST00000652225.2:c.1707T>C (ERCC5) MANE Select	ENSP00000498881.2:p.Cys569=
ENST00000652613.1:c.1203T>C (ERCC5)	ENSP00000498357.1:p.Cys401=
ENST00000355739.8:c.1707T>C (ERCC5)	ENSP00000347978.4:p.Cys569=
ENST00000602836.1:c.2983T>C (BIVM-ERCC5)
ENST00000610537.4:c.1707T>C (ERCC5)	ENSP00000478667.1:p.Cys569=
NM_000123.3:c.1707T>C , LRG_464t1:c.1707T>C (ERCC5)	NP_000114.2:p.Cys569=
NM_001204425.1:c.3069T>C (BIVM-ERCC5)	NP_001191354.1:p.Cys1023=
NM_000123.4:c.1707T>C (ERCC5) MANE Select	NP_000114.3:p.Cys569=
NM_001204425.2:c.3069T>C (BIVM-ERCC5)	NP_001191354.2:p.Cys1023=