Canonical Allele Identifier: CA2216894047

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094624C= , CM000678.2:g.31094624C=	GRCh38
NC_000016.9:g.31105945C= , CM000678.1:g.31105945C=	GRCh37
NC_000016.8:g.31013446C=	NCBI36
NG_011564.1:g.5332G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024006.6:c.106G= MANE Select	NP_076869.1:p.Asp36=
ENST00000394975.3:c.106G= MANE Select	ENSP00000378426.2:p.Asp36=
NM_001311311.1:c.106G=	NP_001298240.1:p.Asp36=
NM_001311311.2:c.106G=	NP_001298240.1:p.Asp36=
NM_024006.4:c.106G=	NP_076869.1:p.Asp36=
NM_024006.5:c.106G=	NP_076869.1:p.Asp36=
NM_206824.1:c.106G=	NP_996560.1:p.Asp36=
NM_206824.2:c.106G=	NP_996560.1:p.Asp36=
NM_206824.3:c.106G=	NP_996560.1:p.Asp36=
ENST00000300851.10:c.106G=	ENSP00000300851.6:p.Asp36=
ENST00000319788.11:c.106G=	ENSP00000326135.7:p.Asp36=
ENST00000354895.4:c.106G=	ENSP00000346969.4:p.Asp36=
ENST00000394975.2:c.106G=	ENSP00000378426.2:p.Asp36=
ENST00000420057.2:c.245+765G=
ENST00000498155.1:c.270+765G=	ENSP00000417662.1:n.270+765G=
ENST00000529564.1:c.106G=	ENSP00000431371.1:p.Asp36=
ENST00000532364.1:c.106G=	ENSP00000460316.1:p.Asp36=
XM_011545944.1:c.106G=	XP_011544246.1:p.Asp36=
XM_011545945.1:c.106G=	XP_011544247.1:p.Asp36=
XR_950848.1:n.894G=