Canonical Allele Identifier: CA2216889057

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091203G= , CM000678.2:g.31091203G=	GRCh38
NC_000016.9:g.31102524G= , CM000678.1:g.31102524G=	GRCh37
NC_000016.8:g.31010025G=	NCBI36
NG_011564.1:g.8753C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.423C= MANE Select	ENSP00000378426.2:p.Ile141=
ENST00000300851.10:c.*34C=	ENSP00000300851.6:n.*34C=
ENST00000319788.11:c.*34C=	ENSP00000326135.7:n.*34C=
ENST00000354895.4:c.*34C=	ENSP00000346969.4:n.*34C=
ENST00000394971.7:c.*34C=	ENSP00000378422.3:n.*34C=
ENST00000394975.2:c.423C=	ENSP00000378426.2:p.Ile141=
ENST00000420057.2:c.385C=
ENST00000472468.1:c.108C=	ENSP00000458994.1:p.Ile36=
ENST00000498155.1:c.*34C=	ENSP00000417662.1:n.*34C=
ENST00000529564.1:c.283+2109C=	ENSP00000431371.1:n.283+2109C=
ENST00000532364.1:c.173+3354C=	ENSP00000460316.1:n.173+3354C=
ENST00000533518.5:c.296C=
NM_001311311.1:c.507C=	NP_001298240.1:p.Ile169=
NM_024006.4:c.423C=	NP_076869.1:p.Ile141=
NM_024006.5:c.423C=	NP_076869.1:p.Ile141=
NM_206824.1:c.*34C=	NP_996560.1:n.*34C=
NM_206824.2:c.*34C=	NP_996560.1:n.*34C=
XM_011545944.1:c.423C=	XP_011544246.1:p.Ile141=
XM_011545945.1:c.*34C=	XP_011544247.1:n.*34C=
XR_950848.1:n.1211C=
NM_024006.6:c.423C= MANE Select	NP_076869.1:p.Ile141=
NM_001311311.2:c.507C=	NP_001298240.1:p.Ile169=
NM_206824.3:c.*34C=	NP_996560.1:n.*34C=