Canonical Allele Identifier: CA2216888920

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091119G= , CM000678.2:g.31091119G=	GRCh38
NC_000016.9:g.31102440G= , CM000678.1:g.31102440G=	GRCh37
NC_000016.8:g.31009941G=	NCBI36
NG_011564.1:g.8837C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.*15C= MANE Select	ENSP00000378426.2:n.*15C=
ENST00000300851.10:c.*118C=	ENSP00000300851.6:n.*118C=
ENST00000319788.11:c.*118C=	ENSP00000326135.7:n.*118C=
ENST00000354895.4:c.*118C=	ENSP00000346969.4:n.*118C=
ENST00000394971.7:c.*118C=	ENSP00000378422.3:n.*118C=
ENST00000394975.2:c.*15C=	ENSP00000378426.2:n.*15C=
ENST00000420057.2:c.469C=
ENST00000529564.1:c.283+2193C=	ENSP00000431371.1:n.283+2193C=
ENST00000532364.1:c.173+3438C=	ENSP00000460316.1:n.173+3438C=
ENST00000533518.5:c.380C=
NM_001311311.1:c.*15C=	NP_001298240.1:n.*15C=
NM_024006.4:c.*15C=	NP_076869.1:n.*15C=
NM_024006.5:c.*15C=	NP_076869.1:n.*15C=
NM_206824.1:c.*118C=	NP_996560.1:n.*118C=
NM_206824.2:c.*118C=	NP_996560.1:n.*118C=
XM_011545944.1:c.*15C=	XP_011544246.1:n.*15C=
XM_011545945.1:c.*118C=	XP_011544247.1:n.*118C=
XR_950848.1:n.1295C=
NM_024006.6:c.*15C= MANE Select	NP_076869.1:n.*15C=
NM_001311311.2:c.*15C=	NP_001298240.1:n.*15C=
NM_206824.3:c.*118C=	NP_996560.1:n.*118C=