Canonical Allele Identifier: CA376721328

Gene: ERCC6

Linked Data

• ClinVar Variation Id: 522698
• ClinVar RCV Id: RCV000625851 ; RCV001855324
• dbSNP Id: rs368728467
• MyVariant Identifiers: chr10:g.50682120A>T (hg19) ; chr10:g.49474074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49474074A>T , CM000672.2:g.49474074A>T	GRCh38
NC_000010.10:g.50682120A>T , CM000672.1:g.50682120A>T	GRCh37
NC_000010.9:g.50352126A>T	NCBI36
NG_009442.1:g.70028T>A , LRG_465:g.70028T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2551T>A MANE Select	ENSP00000348089.5:p.Trp851Arg
ENST00000681632.1:n.2629T>A
ENST00000681659.1:c.2392T>A	ENSP00000505631.1:p.Trp798Arg
ENST00000355832.9:c.2551T>A	ENSP00000348089.5:p.Trp851Arg
ENST00000623073.3:c.*847T>A	ENSP00000485650.1:n.*847T>A
ENST00000623115.3:c.661T>A	ENSP00000485321.1:p.Trp221Arg
ENST00000624341.3:c.383T>A
NM_000124.3:c.2551T>A	NP_000115.1:p.Trp851Arg
NM_001346440.1:c.2551T>A	NP_001333369.1:p.Trp851Arg
NM_000124.4:c.2551T>A MANE Select	NP_000115.1:p.Trp851Arg
NM_001346440.2:c.2551T>A	NP_001333369.1:p.Trp851Arg