Canonical Allele Identifier: CA388574067

Gene: ERCC5 BIVM-ERCC5

Linked Data

• MyVariant Identifiers: chr13:g.103515204T>A (hg19) ; chr13:g.102862854T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.102862854T>A , CM000675.2:g.102862854T>A	GRCh38
NC_000013.10:g.103515204T>A , CM000675.1:g.103515204T>A	GRCh37
NC_000013.9:g.102313205T>A	NCBI36
NG_007146.1:g.22031T>A , LRG_464:g.22031T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682632.1:n.1946T>A (ERCC5)
ENST00000682869.1:n.2354T>A (ERCC5)
ENST00000683246.1:n.2482T>A (ERCC5)
ENST00000639132.1:c.2380T>A (BIVM-ERCC5)	ENSP00000492684.1:p.Cys794Ser
ENST00000639435.1:c.3067T>A (BIVM-ERCC5)	ENSP00000491742.1:p.Cys1023Ser
ENST00000651002.1:c.*1466T>A (ERCC5)	ENSP00000498809.1:n.*1466T>A
ENST00000651055.1:n.1834T>A (ERCC5)
ENST00000651281.1:n.2073T>A (ERCC5)
ENST00000651387.1:n.1189T>A (ERCC5)
ENST00000651470.1:c.1705T>A (ERCC5)	ENSP00000498701.1:p.Cys569Ser
ENST00000652225.2:c.1705T>A (ERCC5) MANE Select	ENSP00000498881.2:p.Cys569Ser
ENST00000652613.1:c.1201T>A (ERCC5)	ENSP00000498357.1:p.Cys401Ser
ENST00000355739.8:c.1705T>A (ERCC5)	ENSP00000347978.4:p.Cys569Ser
ENST00000602836.1:c.2981T>A (BIVM-ERCC5)
ENST00000610537.4:c.1705T>A (ERCC5)	ENSP00000478667.1:p.Cys569Ser
NM_000123.3:c.1705T>A , LRG_464t1:c.1705T>A (ERCC5)	NP_000114.2:p.Cys569Ser
NM_001204425.1:c.3067T>A (BIVM-ERCC5)	NP_001191354.1:p.Cys1023Ser
NM_000123.4:c.1705T>A (ERCC5) MANE Select	NP_000114.3:p.Cys569Ser
NM_001204425.2:c.3067T>A (BIVM-ERCC5)	NP_001191354.2:p.Cys1023Ser