Canonical Allele Identifier: CA2216889323
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091335C= , CM000678.2:g.31091335C= GRCh38
NC_000016.9:g.31102656C= , CM000678.1:g.31102656C= GRCh37
NC_000016.8:g.31010157C= NCBI36
NG_011564.1:g.8621G=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.291G= MANE Select ENSP00000378426.2:p.Leu97=
ENST00000300851.10:c.352G= ENSP00000300851.6:p.Ala118=
ENST00000319788.11:c.373G= ENSP00000326135.7:p.Ala125=
ENST00000354895.4:c.181G= ENSP00000346969.4:p.Ala61=
ENST00000394971.7:c.385G= ENSP00000378422.3:p.Ala129=
ENST00000394975.2:c.291G= ENSP00000378426.2:p.Leu97=
ENST00000420057.2:c.253G=
ENST00000472468.1:c.-25G= ENSP00000458994.1:n.-25G=
ENST00000498155.1:c.388G= ENSP00000417662.1:p.Ala130=
ENST00000529564.1:c.283+1977G= ENSP00000431371.1:n.283+1977G=
ENST00000532364.1:c.173+3222G= ENSP00000460316.1:n.173+3222G=
ENST00000533518.5:c.164G=
NM_001311311.1:c.375G= NP_001298240.1:p.Leu125=
NM_024006.4:c.291G= NP_076869.1:p.Leu97=
NM_024006.5:c.291G= NP_076869.1:p.Leu97=
NM_206824.1:c.181G= NP_996560.1:p.Ala61=
NM_206824.2:c.181G= NP_996560.1:p.Ala61=
XM_011545944.1:c.291G= XP_011544246.1:p.Leu97=
XM_011545945.1:c.181G= XP_011544247.1:p.Ala61=
XR_950848.1:n.1079G=
NM_024006.6:c.291G= MANE Select NP_076869.1:p.Leu97=
NM_001311311.2:c.375G= NP_001298240.1:p.Leu125=
NM_206824.3:c.181G= NP_996560.1:p.Ala61=