Canonical Allele Identifier: CA2216889276

Gene: VKORC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091310T= , CM000678.2:g.31091310T=	GRCh38
NC_000016.9:g.31102631T= , CM000678.1:g.31102631T=	GRCh37
NC_000016.8:g.31010132T=	NCBI36
NG_011564.1:g.8646A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.316A= MANE Select	ENSP00000378426.2:p.Met106=
ENST00000300851.10:c.377A=	ENSP00000300851.6:p.Asp126=
ENST00000319788.11:c.398A=	ENSP00000326135.7:p.Asp133=
ENST00000354895.4:c.206A=	ENSP00000346969.4:p.Asp69=
ENST00000394971.7:c.410A=	ENSP00000378422.3:p.Asp137=
ENST00000394975.2:c.316A=	ENSP00000378426.2:p.Met106=
ENST00000420057.2:c.278A=
ENST00000472468.1:c.1A=	ENSP00000458994.1:p.Met1=
ENST00000498155.1:c.413A=	ENSP00000417662.1:p.Asp138=
ENST00000529564.1:c.283+2002A=	ENSP00000431371.1:n.283+2002A=
ENST00000532364.1:c.173+3247A=	ENSP00000460316.1:n.173+3247A=
ENST00000533518.5:c.189A=
NM_001311311.1:c.400A=	NP_001298240.1:p.Met134=
NM_024006.4:c.316A=	NP_076869.1:p.Met106=
NM_024006.5:c.316A=	NP_076869.1:p.Met106=
NM_206824.1:c.206A=	NP_996560.1:p.Asp69=
NM_206824.2:c.206A=	NP_996560.1:p.Asp69=
XM_011545944.1:c.316A=	XP_011544246.1:p.Met106=
XM_011545945.1:c.206A=	XP_011544247.1:p.Asp69=
XR_950848.1:n.1104A=
NM_024006.6:c.316A= MANE Select	NP_076869.1:p.Met106=
NM_001311311.2:c.400A=	NP_001298240.1:p.Met134=
NM_206824.3:c.206A=	NP_996560.1:p.Asp69=