Canonical Allele Identifier: CA658798593

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31103796A>A (hg19) ; chr16:g.31092475A>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31092475A= , CM000678.2:g.31092475A=	GRCh38
NC_000016.9:g.31103796A= , CM000678.1:g.31103796A=	GRCh37
NC_000016.8:g.31011297A=	NCBI36
NG_011564.1:g.7481T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394975.3:c.283+837T= MANE Select	ENSP00000378426.2:n.283+837T=
ENST00000300851.10:c.344+837T=	ENSP00000300851.6:n.344+837T=
ENST00000319788.11:c.365+308T=	ENSP00000326135.7:n.365+308T=
ENST00000354895.4:c.174-1133T=	ENSP00000346969.4:n.174-1133T=
ENST00000394971.7:c.377+837T=	ENSP00000378422.3:n.377+837T=
ENST00000394975.2:c.283+837T=	ENSP00000378426.2:n.283+837T=
ENST00000420057.2:c.246-1133T=
ENST00000472468.1:c.-33+837T=	ENSP00000458994.1:n.-33+837T=
ENST00000498155.1:c.380+837T=	ENSP00000417662.1:n.380+837T=
ENST00000529564.1:c.283+837T=	ENSP00000431371.1:n.283+837T=
ENST00000532364.1:c.173+2082T=	ENSP00000460316.1:n.173+2082T=
ENST00000533518.5:c.156+837T=
NM_001311311.1:c.367+308T=	NP_001298240.1:n.367+308T=
NM_024006.4:c.283+837T=	NP_076869.1:n.283+837T=
NM_024006.5:c.283+837T=	NP_076869.1:n.283+837T=
NM_206824.1:c.174-1133T=	NP_996560.1:n.174-1133T=
NM_206824.2:c.174-1133T=	NP_996560.1:n.174-1133T=
XM_011545944.1:c.283+837T=	XP_011544246.1:n.283+837T=
XM_011545945.1:c.174-1133T=	XP_011544247.1:n.174-1133T=
XR_950848.1:n.1071+837T=
NM_024006.6:c.283+837T= MANE Select	NP_076869.1:n.283+837T=
NM_001311311.2:c.367+308T=	NP_001298240.1:n.367+308T=
NM_206824.3:c.174-1133T=	NP_996560.1:n.174-1133T=