Canonical Allele Identifier: CA2216889164

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091268G= , CM000678.2:g.31091268G=	GRCh38
NC_000016.9:g.31102589G= , CM000678.1:g.31102589G=	GRCh37
NC_000016.8:g.31010090G=	NCBI36
NG_011564.1:g.8688C=

Transcript Alleles

HGVS	Amino-acid Change
NM_024006.6:c.358C= MANE Select	NP_076869.1:p.Leu120=
ENST00000394975.3:c.358C= MANE Select	ENSP00000378426.2:p.Leu120=
NM_001311311.1:c.442C=	NP_001298240.1:p.Leu148=
NM_001311311.2:c.442C=	NP_001298240.1:p.Leu148=
NM_024006.4:c.358C=	NP_076869.1:p.Leu120=
NM_024006.5:c.358C=	NP_076869.1:p.Leu120=
NM_206824.1:c.248C=	NP_996560.1:p.Pro83=
NM_206824.2:c.248C=	NP_996560.1:p.Pro83=
NM_206824.3:c.248C=	NP_996560.1:p.Pro83=
ENST00000300851.10:c.419C=	ENSP00000300851.6:p.Pro140=
ENST00000319788.11:c.440C=	ENSP00000326135.7:p.Pro147=
ENST00000354895.4:c.248C=	ENSP00000346969.4:p.Pro83=
ENST00000394971.7:c.452C=	ENSP00000378422.3:p.Pro151=
ENST00000394975.2:c.358C=	ENSP00000378426.2:p.Leu120=
ENST00000420057.2:c.320C=
ENST00000472468.1:c.43C=	ENSP00000458994.1:p.Leu15=
ENST00000498155.1:c.455C=	ENSP00000417662.1:p.Pro152=
ENST00000529564.1:c.283+2044C=	ENSP00000431371.1:n.283+2044C=
ENST00000532364.1:c.173+3289C=	ENSP00000460316.1:n.173+3289C=
ENST00000533518.5:c.231C=
XM_011545944.1:c.358C=	XP_011544246.1:p.Leu120=
XM_011545945.1:c.248C=	XP_011544247.1:p.Pro83=
XR_950848.1:n.1146C=