Canonical Allele Identifier: CA388673421

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs1883092487
• MyVariant Identifiers: chr13:g.103525611T>A (hg19) ; chr13:g.102873261T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102873261T>A , CM000675.2:g.102873261T>A	GRCh38
NC_000013.10:g.103525611T>A , CM000675.1:g.103525611T>A	GRCh37
NC_000013.9:g.102323612T>A	NCBI36
NG_007146.1:g.32438T>A , LRG_464:g.32438T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.3983T>A (ERCC5)
ENST00000682869.1:n.3531T>A (ERCC5)
ENST00000683246.1:n.4519T>A (ERCC5)
ENST00000683642.1:n.3112T>A (ERCC5)
ENST00000639132.1:c.3557T>A (BIVM-ERCC5)	ENSP00000492684.1:p.Phe1186Tyr
ENST00000639435.1:c.4244T>A (BIVM-ERCC5)	ENSP00000491742.1:p.Phe1415Tyr
ENST00000651002.1:c.*2643T>A (ERCC5)	ENSP00000498809.1:n.*2643T>A
ENST00000651055.1:n.3009T>A (ERCC5)
ENST00000651281.1:n.3250T>A (ERCC5)
ENST00000651387.1:n.2366T>A (ERCC5)
ENST00000651470.1:c.*54T>A (ERCC5)	ENSP00000498701.1:n.*54T>A
ENST00000652225.2:c.2882T>A (ERCC5) MANE Select	ENSP00000498881.2:p.Phe961Tyr
ENST00000652613.1:c.2378T>A (ERCC5)	ENSP00000498357.1:p.Phe793Tyr
ENST00000355739.8:c.2882T>A (ERCC5)	ENSP00000347978.4:p.Phe961Tyr
ENST00000375954.1:c.581T>A (ERCC5)	ENSP00000365121.1:p.Phe194Tyr
ENST00000610537.4:c.2879T>A (ERCC5)	ENSP00000478667.1:p.Phe960Tyr
NM_000123.3:c.2882T>A , LRG_464t1:c.2882T>A (ERCC5)	NP_000114.2:p.Phe961Tyr
NM_001204425.1:c.4244T>A (BIVM-ERCC5)	NP_001191354.1:p.Phe1415Tyr
NM_000123.4:c.2882T>A (ERCC5) MANE Select	NP_000114.3:p.Phe961Tyr
NM_001204425.2:c.4244T>A (BIVM-ERCC5)	NP_001191354.2:p.Phe1415Tyr