Canonical Allele Identifier: CA388576334

Gene: ERCC5 BIVM-ERCC5

Linked Data

• dbSNP Id: rs2140532561
• MyVariant Identifiers: chr13:g.103519049T>C (hg19) ; chr13:g.102866699T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102866699T>C , CM000675.2:g.102866699T>C	GRCh38
NC_000013.10:g.103519049T>C , CM000675.1:g.103519049T>C	GRCh37
NC_000013.9:g.102317050T>C	NCBI36
NG_007146.1:g.25876T>C , LRG_464:g.25876T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.2628T>C (ERCC5)
ENST00000682869.1:n.3036T>C (ERCC5)
ENST00000683246.1:n.3164T>C (ERCC5)
ENST00000639132.1:c.3062T>C (BIVM-ERCC5)	ENSP00000492684.1:p.Ile1021Thr
ENST00000639435.1:c.3749T>C (BIVM-ERCC5)	ENSP00000491742.1:p.Ile1250Thr
ENST00000651002.1:c.*2148T>C (ERCC5)	ENSP00000498809.1:n.*2148T>C
ENST00000651055.1:n.2516T>C (ERCC5)
ENST00000651281.1:n.2755T>C (ERCC5)
ENST00000651387.1:n.1871T>C (ERCC5)
ENST00000651470.1:c.2387T>C (ERCC5)	ENSP00000498701.1:p.Ile796Thr
ENST00000652225.2:c.2387T>C (ERCC5) MANE Select	ENSP00000498881.2:p.Ile796Thr
ENST00000652613.1:c.1883T>C (ERCC5)	ENSP00000498357.1:p.Ile628Thr
ENST00000355739.8:c.2387T>C (ERCC5)	ENSP00000347978.4:p.Ile796Thr
ENST00000375954.1:c.86T>C (ERCC5)	ENSP00000365121.1:p.Ile29Thr
ENST00000481099.1:n.507T>C (ERCC5)
ENST00000602836.1:c.3663T>C (BIVM-ERCC5)
ENST00000610537.4:c.2387T>C (ERCC5)	ENSP00000478667.1:p.Ile796Thr
NM_000123.3:c.2387T>C , LRG_464t1:c.2387T>C (ERCC5)	NP_000114.2:p.Ile796Thr
NM_001204425.1:c.3749T>C (BIVM-ERCC5)	NP_001191354.1:p.Ile1250Thr
NM_000123.4:c.2387T>C (ERCC5) MANE Select	NP_000114.3:p.Ile796Thr
NM_001204425.2:c.3749T>C (BIVM-ERCC5)	NP_001191354.2:p.Ile1250Thr