Canonical Allele Identifier: CA1908745534

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461532T= , CM000672.2:g.49461532T=	GRCh38
NC_000010.10:g.50669578T= , CM000672.1:g.50669578T=	GRCh37
NC_000010.9:g.50339584T=	NCBI36
NG_009442.1:g.82570A= , LRG_465:g.82570A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3803A= MANE Select	ENSP00000348089.5:p.His1268=
ENST00000679552.1:n.874A=
ENST00000679871.1:n.949A=
ENST00000679974.1:n.852A=
ENST00000681632.1:n.5206A=
ENST00000681659.1:c.3644A=	ENSP00000505631.1:p.His1215=
ENST00000355832.9:c.3803A=	ENSP00000348089.5:p.His1268=
ENST00000465653.1:n.125A=
ENST00000623073.3:c.*2099A=	ENSP00000485650.1:n.*2099A=
ENST00000623115.3:c.1913A=	ENSP00000485321.1:p.His638=
ENST00000624341.3:c.1635A=
NM_000124.3:c.3803A=	NP_000115.1:p.His1268=
XR_945953.1:n.243-10033T=
NM_001346440.1:c.3803A=	NP_001333369.1:p.His1268=
NM_000124.4:c.3803A= MANE Select	NP_000115.1:p.His1268=
NM_001346440.2:c.3803A=	NP_001333369.1:p.His1268=