Canonical Allele Identifier: CA376708259

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669429T>A (hg19) ; chr10:g.49461383T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461383T>A , CM000672.2:g.49461383T>A	GRCh38
NC_000010.10:g.50669429T>A , CM000672.1:g.50669429T>A	GRCh37
NC_000010.9:g.50339435T>A	NCBI36
NG_009442.1:g.82719A>T , LRG_465:g.82719A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.3952A>T MANE Select	ENSP00000348089.5:p.Arg1318Trp
ENST00000679552.1:n.1023A>T
ENST00000679871.1:n.1098A>T
ENST00000679974.1:n.1001A>T
ENST00000681632.1:n.5355A>T
ENST00000681659.1:c.3793A>T	ENSP00000505631.1:p.Arg1265Trp
ENST00000355832.9:c.3952A>T	ENSP00000348089.5:p.Arg1318Trp
ENST00000465653.1:n.274A>T
ENST00000623073.3:c.*2248A>T	ENSP00000485650.1:n.*2248A>T
ENST00000623115.3:c.2062A>T	ENSP00000485321.1:p.Arg688Trp
ENST00000624341.3:c.1784A>T
NM_000124.3:c.3952A>T	NP_000115.1:p.Arg1318Trp
XR_945953.1:n.243-10182T>A
NM_001346440.1:c.3952A>T	NP_001333369.1:p.Arg1318Trp
NM_000124.4:c.3952A>T MANE Select	NP_000115.1:p.Arg1318Trp
NM_001346440.2:c.3952A>T	NP_001333369.1:p.Arg1318Trp