Canonical Allele Identifier: CA2216888504

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31090859G= , CM000678.2:g.31090859G=	GRCh38
NC_000016.9:g.31102180G= , CM000678.1:g.31102180G=	GRCh37
NC_000016.8:g.31009681G=	NCBI36
NG_011564.1:g.9097C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*275C= MANE Select	ENSP00000378426.2:n.*275C=
ENST00000300851.10:c.*378C=	ENSP00000300851.6:n.*378C=
ENST00000319788.11:c.*378C=	ENSP00000326135.7:n.*378C=
ENST00000354895.4:c.*378C=	ENSP00000346969.4:n.*378C=
ENST00000394975.2:c.*275C=	ENSP00000378426.2:n.*275C=
ENST00000420057.2:c.729C=
ENST00000529564.1:c.283+2453C=	ENSP00000431371.1:n.283+2453C=
ENST00000532364.1:c.173+3698C=	ENSP00000460316.1:n.173+3698C=
ENST00000533518.5:c.407+233C=
NM_001311311.1:c.*275C=	NP_001298240.1:n.*275C=
NM_024006.4:c.*275C=	NP_076869.1:n.*275C=
NM_024006.5:c.*275C=	NP_076869.1:n.*275C=
NM_206824.1:c.*378C=	NP_996560.1:n.*378C=
NM_206824.2:c.*378C=	NP_996560.1:n.*378C=
XM_011545944.1:c.*275C=	XP_011544246.1:n.*275C=
XM_011545945.1:c.*378C=	XP_011544247.1:n.*378C=
XR_950848.1:n.1555C=
NM_024006.6:c.*275C= MANE Select	NP_076869.1:n.*275C=
NM_001311311.2:c.*275C=	NP_001298240.1:n.*275C=
NM_206824.3:c.*378C=	NP_996560.1:n.*378C=