Canonical Allele Identifier: CA494926044

Gene: VKORC1

Linked Data

• MyVariant Identifiers: chr16:g.31102662A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31091341A>G , CM000678.2:g.31091341A>G	GRCh38
NC_000016.9:g.31102662A>G , CM000678.1:g.31102662A>G	GRCh37
NC_000016.8:g.31010163A>G	NCBI36
NG_011564.1:g.8615T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394975.3:c.285T>C MANE Select	ENSP00000378426.2:p.Gly95=
ENST00000300851.10:c.346T>C	ENSP00000300851.6:p.Leu116=
ENST00000319788.11:c.367T>C	ENSP00000326135.7:p.Leu123=
ENST00000354895.4:c.175T>C	ENSP00000346969.4:p.Leu59=
ENST00000394971.7:c.379T>C	ENSP00000378422.3:p.Leu127=
ENST00000394975.2:c.285T>C	ENSP00000378426.2:p.Gly95=
ENST00000420057.2:c.247T>C
ENST00000472468.1:c.-31T>C	ENSP00000458994.1:n.-31T>C
ENST00000498155.1:c.382T>C	ENSP00000417662.1:p.Leu128=
ENST00000529564.1:c.283+1971T>C	ENSP00000431371.1:n.283+1971T>C
ENST00000532364.1:c.173+3216T>C	ENSP00000460316.1:n.173+3216T>C
ENST00000533518.5:c.158T>C
NM_001311311.1:c.369T>C	NP_001298240.1:p.Arg123=
NM_024006.4:c.285T>C	NP_076869.1:p.Gly95=
NM_024006.5:c.285T>C	NP_076869.1:p.Gly95=
NM_206824.1:c.175T>C	NP_996560.1:p.Leu59=
NM_206824.2:c.175T>C	NP_996560.1:p.Leu59=
XM_011545944.1:c.285T>C	XP_011544246.1:p.Gly95=
XM_011545945.1:c.175T>C	XP_011544247.1:p.Leu59=
XR_950848.1:n.1073T>C
NM_024006.6:c.285T>C MANE Select	NP_076869.1:p.Gly95=
NM_001311311.2:c.369T>C	NP_001298240.1:p.Arg123=
NM_206824.3:c.175T>C	NP_996560.1:p.Leu59=