Canonical Allele Identifier: CA2216888825

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091068C= , CM000678.2:g.31091068C=	GRCh38
NC_000016.9:g.31102389C= , CM000678.1:g.31102389C=	GRCh37
NC_000016.8:g.31009890C=	NCBI36
NG_011564.1:g.8888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*66G= MANE Select	ENSP00000378426.2:n.*66G=
ENST00000300851.10:c.*169G=	ENSP00000300851.6:n.*169G=
ENST00000319788.11:c.*169G=	ENSP00000326135.7:n.*169G=
ENST00000354895.4:c.*169G=	ENSP00000346969.4:n.*169G=
ENST00000394975.2:c.*66G=	ENSP00000378426.2:n.*66G=
ENST00000420057.2:c.520G=
ENST00000529564.1:c.283+2244G=	ENSP00000431371.1:n.283+2244G=
ENST00000532364.1:c.173+3489G=	ENSP00000460316.1:n.173+3489G=
ENST00000533518.5:c.407+24G=
NM_001311311.1:c.*66G=	NP_001298240.1:n.*66G=
NM_024006.4:c.*66G=	NP_076869.1:n.*66G=
NM_024006.5:c.*66G=	NP_076869.1:n.*66G=
NM_206824.1:c.*169G=	NP_996560.1:n.*169G=
NM_206824.2:c.*169G=	NP_996560.1:n.*169G=
XM_011545944.1:c.*66G=	XP_011544246.1:n.*66G=
XM_011545945.1:c.*169G=	XP_011544247.1:n.*169G=
XR_950848.1:n.1346G=
NM_024006.6:c.*66G= MANE Select	NP_076869.1:n.*66G=
NM_001311311.2:c.*66G=	NP_001298240.1:n.*66G=
NM_206824.3:c.*169G=	NP_996560.1:n.*169G=