Canonical Allele Identifier: CA2216889300

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091327C= , CM000678.2:g.31091327C=	GRCh38
NC_000016.9:g.31102648C= , CM000678.1:g.31102648C=	GRCh37
NC_000016.8:g.31010149C=	NCBI36
NG_011564.1:g.8629G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.299G= MANE Select	ENSP00000378426.2:p.Arg100=
ENST00000300851.10:c.360G=	ENSP00000300851.6:p.Thr120=
ENST00000319788.11:c.381G=	ENSP00000326135.7:p.Thr127=
ENST00000354895.4:c.189G=	ENSP00000346969.4:p.Thr63=
ENST00000394971.7:c.393G=	ENSP00000378422.3:p.Thr131=
ENST00000394975.2:c.299G=	ENSP00000378426.2:p.Arg100=
ENST00000420057.2:c.261G=
ENST00000472468.1:c.-17G=	ENSP00000458994.1:n.-17G=
ENST00000498155.1:c.396G=	ENSP00000417662.1:p.Thr132=
ENST00000529564.1:c.283+1985G=	ENSP00000431371.1:n.283+1985G=
ENST00000532364.1:c.173+3230G=	ENSP00000460316.1:n.173+3230G=
ENST00000533518.5:c.172G=
NM_001311311.1:c.383G=	NP_001298240.1:p.Arg128=
NM_024006.4:c.299G=	NP_076869.1:p.Arg100=
NM_024006.5:c.299G=	NP_076869.1:p.Arg100=
NM_206824.1:c.189G=	NP_996560.1:p.Thr63=
NM_206824.2:c.189G=	NP_996560.1:p.Thr63=
XM_011545944.1:c.299G=	XP_011544246.1:p.Arg100=
XM_011545945.1:c.189G=	XP_011544247.1:p.Thr63=
XR_950848.1:n.1087G=
NM_024006.6:c.299G= MANE Select	NP_076869.1:p.Arg100=
NM_001311311.2:c.383G=	NP_001298240.1:p.Arg128=
NM_206824.3:c.189G=	NP_996560.1:p.Thr63=