Canonical Allele Identifier: CA2216889329
Gene: VKORC1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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