Canonical Allele Identifier: CA2216889269

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091300C= , CM000678.2:g.31091300C=	GRCh38
NC_000016.9:g.31102621C= , CM000678.1:g.31102621C=	GRCh37
NC_000016.8:g.31010122C=	NCBI36
NG_011564.1:g.8656G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.326G= MANE Select	ENSP00000378426.2:p.Ser109=
ENST00000300851.10:c.387G=	ENSP00000300851.6:p.Glu129=
ENST00000319788.11:c.408G=	ENSP00000326135.7:p.Glu136=
ENST00000354895.4:c.216G=	ENSP00000346969.4:p.Glu72=
ENST00000394971.7:c.420G=	ENSP00000378422.3:p.Glu140=
ENST00000394975.2:c.326G=	ENSP00000378426.2:p.Ser109=
ENST00000420057.2:c.288G=
ENST00000472468.1:c.11G=	ENSP00000458994.1:p.Ser4=
ENST00000498155.1:c.423G=	ENSP00000417662.1:p.Glu141=
ENST00000529564.1:c.283+2012G=	ENSP00000431371.1:n.283+2012G=
ENST00000532364.1:c.173+3257G=	ENSP00000460316.1:n.173+3257G=
ENST00000533518.5:c.199G=
NM_001311311.1:c.410G=	NP_001298240.1:p.Ser137=
NM_024006.4:c.326G=	NP_076869.1:p.Ser109=
NM_024006.5:c.326G=	NP_076869.1:p.Ser109=
NM_206824.1:c.216G=	NP_996560.1:p.Glu72=
NM_206824.2:c.216G=	NP_996560.1:p.Glu72=
XM_011545944.1:c.326G=	XP_011544246.1:p.Ser109=
XM_011545945.1:c.216G=	XP_011544247.1:p.Glu72=
XR_950848.1:n.1114G=
NM_024006.6:c.326G= MANE Select	NP_076869.1:p.Ser109=
NM_001311311.2:c.410G=	NP_001298240.1:p.Ser137=
NM_206824.3:c.216G=	NP_996560.1:p.Glu72=