Canonical Allele Identifier: CA255466902

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs906636265
• MyVariant Identifiers: chr13:g.103525623A>G (hg19) ; chr13:g.102873273A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873273A>G , CM000675.2:g.102873273A>G	GRCh38
NC_000013.10:g.103525623A>G , CM000675.1:g.103525623A>G	GRCh37
NC_000013.9:g.102323624A>G	NCBI36
NG_007146.1:g.32450A>G , LRG_464:g.32450A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.3995A>G (ERCC5)
ENST00000682869.1:n.3543A>G (ERCC5)
ENST00000683246.1:n.4531A>G (ERCC5)
ENST00000683642.1:n.3124A>G (ERCC5)
ENST00000639132.1:c.3569A>G (BIVM-ERCC5)	ENSP00000492684.1:p.Tyr1190Cys
ENST00000639435.1:c.4256A>G (BIVM-ERCC5)	ENSP00000491742.1:p.Tyr1419Cys
ENST00000651002.1:c.*2655A>G (ERCC5)	ENSP00000498809.1:n.*2655A>G
ENST00000651055.1:n.3021A>G (ERCC5)
ENST00000651281.1:n.3262A>G (ERCC5)
ENST00000651387.1:n.2378A>G (ERCC5)
ENST00000651470.1:c.*66A>G (ERCC5)	ENSP00000498701.1:n.*66A>G
ENST00000652225.2:c.2894A>G (ERCC5) MANE Select	ENSP00000498881.2:p.Tyr965Cys
ENST00000652613.1:c.2390A>G (ERCC5)	ENSP00000498357.1:p.Tyr797Cys
ENST00000355739.8:c.2894A>G (ERCC5)	ENSP00000347978.4:p.Tyr965Cys
ENST00000375954.1:c.593A>G (ERCC5)	ENSP00000365121.1:p.Tyr198Cys
ENST00000610537.4:c.2891A>G (ERCC5)	ENSP00000478667.1:p.Tyr964Cys
NM_000123.3:c.2894A>G , LRG_464t1:c.2894A>G (ERCC5)	NP_000114.2:p.Tyr965Cys
NM_001204425.1:c.4256A>G (BIVM-ERCC5)	NP_001191354.1:p.Tyr1419Cys
NM_000123.4:c.2894A>G (ERCC5) MANE Select	NP_000114.3:p.Tyr965Cys
NM_001204425.2:c.4256A>G (BIVM-ERCC5)	NP_001191354.2:p.Tyr1419Cys