Canonical Allele Identifier: CA1908745454
Gene: ERCC6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.3952A= MANE Select ENSP00000348089.5:p.Arg1318=
ENST00000679552.1:n.1023A=
ENST00000679871.1:n.1098A=
ENST00000679974.1:n.1001A=
ENST00000681632.1:n.5355A=
ENST00000681659.1:c.3793A= ENSP00000505631.1:p.Arg1265=
ENST00000355832.9:c.3952A= ENSP00000348089.5:p.Arg1318=
ENST00000465653.1:n.274A=
ENST00000623073.3:c.*2248A= ENSP00000485650.1:n.*2248A=
ENST00000623115.3:c.2062A= ENSP00000485321.1:p.Arg688=
ENST00000624341.3:c.1784A=
NM_000124.3:c.3952A= NP_000115.1:p.Arg1318=
XR_945953.1:n.243-10182T=
NM_001346440.1:c.3952A= NP_001333369.1:p.Arg1318=
NM_000124.4:c.3952A= MANE Select NP_000115.1:p.Arg1318=
NM_001346440.2:c.3952A= NP_001333369.1:p.Arg1318=