Canonical Allele Identifier: CA2216889318

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091334G= , CM000678.2:g.31091334G=	GRCh38
NC_000016.9:g.31102655G= , CM000678.1:g.31102655G=	GRCh37
NC_000016.8:g.31010156G=	NCBI36
NG_011564.1:g.8622C=

Transcript Alleles

HGVS	Amino-acid Change
NM_024006.6:c.292C= MANE Select	NP_076869.1:p.Arg98=
ENST00000394975.3:c.292C= MANE Select	ENSP00000378426.2:p.Arg98=
NM_001311311.1:c.376C=	NP_001298240.1:p.Arg126=
NM_001311311.2:c.376C=	NP_001298240.1:p.Arg126=
NM_024006.4:c.292C=	NP_076869.1:p.Arg98=
NM_024006.5:c.292C=	NP_076869.1:p.Arg98=
NM_206824.1:c.182C=	NP_996560.1:p.Ala61=
NM_206824.2:c.182C=	NP_996560.1:p.Ala61=
NM_206824.3:c.182C=	NP_996560.1:p.Ala61=
ENST00000300851.10:c.353C=	ENSP00000300851.6:p.Ala118=
ENST00000319788.11:c.374C=	ENSP00000326135.7:p.Ala125=
ENST00000354895.4:c.182C=	ENSP00000346969.4:p.Ala61=
ENST00000394971.7:c.386C=	ENSP00000378422.3:p.Ala129=
ENST00000394975.2:c.292C=	ENSP00000378426.2:p.Arg98=
ENST00000420057.2:c.254C=
ENST00000472468.1:c.-24C=	ENSP00000458994.1:n.-24C=
ENST00000498155.1:c.389C=	ENSP00000417662.1:p.Ala130=
ENST00000529564.1:c.283+1978C=	ENSP00000431371.1:n.283+1978C=
ENST00000532364.1:c.173+3223C=	ENSP00000460316.1:n.173+3223C=
ENST00000533518.5:c.165C=
XM_011545944.1:c.292C=	XP_011544246.1:p.Arg98=
XM_011545945.1:c.182C=	XP_011544247.1:p.Ala61=
XR_950848.1:n.1080C=