Canonical Allele Identifier: CA1908745529

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461517T= , CM000672.2:g.49461517T=	GRCh38
NC_000010.10:g.50669563T= , CM000672.1:g.50669563T=	GRCh37
NC_000010.9:g.50339569T=	NCBI36
NG_009442.1:g.82585A= , LRG_465:g.82585A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3818A= MANE Select	ENSP00000348089.5:p.Asp1273=
ENST00000679552.1:n.889A=
ENST00000679871.1:n.964A=
ENST00000679974.1:n.867A=
ENST00000681632.1:n.5221A=
ENST00000681659.1:c.3659A=	ENSP00000505631.1:p.Asp1220=
ENST00000355832.9:c.3818A=	ENSP00000348089.5:p.Asp1273=
ENST00000465653.1:n.140A=
ENST00000623073.3:c.*2114A=	ENSP00000485650.1:n.*2114A=
ENST00000623115.3:c.1928A=	ENSP00000485321.1:p.Asp643=
ENST00000624341.3:c.1650A=
NM_000124.3:c.3818A=	NP_000115.1:p.Asp1273=
XR_945953.1:n.243-10048T=
NM_001346440.1:c.3818A=	NP_001333369.1:p.Asp1273=
NM_000124.4:c.3818A= MANE Select	NP_000115.1:p.Asp1273=
NM_001346440.2:c.3818A=	NP_001333369.1:p.Asp1273=