Canonical Allele Identifier: CA2216894036

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31094618C= , CM000678.2:g.31094618C=	GRCh38
NC_000016.9:g.31105939C= , CM000678.1:g.31105939C=	GRCh37
NC_000016.8:g.31013440C=	NCBI36
NG_011564.1:g.5338G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.112G= MANE Select	ENSP00000378426.2:p.Asp38=
ENST00000300851.10:c.112G=	ENSP00000300851.6:p.Asp38=
ENST00000319788.11:c.112G=	ENSP00000326135.7:p.Asp38=
ENST00000354895.4:c.112G=	ENSP00000346969.4:p.Asp38=
ENST00000394975.2:c.112G=	ENSP00000378426.2:p.Asp38=
ENST00000420057.2:c.245+771G=
ENST00000498155.1:c.270+771G=	ENSP00000417662.1:n.270+771G=
ENST00000529564.1:c.112G=	ENSP00000431371.1:p.Asp38=
ENST00000532364.1:c.112G=	ENSP00000460316.1:p.Asp38=
NM_001311311.1:c.112G=	NP_001298240.1:p.Asp38=
NM_024006.4:c.112G=	NP_076869.1:p.Asp38=
NM_024006.5:c.112G=	NP_076869.1:p.Asp38=
NM_206824.1:c.112G=	NP_996560.1:p.Asp38=
NM_206824.2:c.112G=	NP_996560.1:p.Asp38=
XM_011545944.1:c.112G=	XP_011544246.1:p.Asp38=
XM_011545945.1:c.112G=	XP_011544247.1:p.Asp38=
XR_950848.1:n.900G=
NM_024006.6:c.112G= MANE Select	NP_076869.1:p.Asp38=
NM_001311311.2:c.112G=	NP_001298240.1:p.Asp38=
NM_206824.3:c.112G=	NP_996560.1:p.Asp38=