Canonical Allele Identifier: CA2216889100
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091240T= , CM000678.2:g.31091240T= GRCh38
NC_000016.9:g.31102561T= , CM000678.1:g.31102561T= GRCh37
NC_000016.8:g.31010062T= NCBI36
NG_011564.1:g.8716A=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.386A= MANE Select ENSP00000378426.2:p.Tyr129=
ENST00000300851.10:c.447A= ENSP00000300851.6:p.Leu149=
ENST00000319788.11:c.468A= ENSP00000326135.7:p.Leu156=
ENST00000354895.4:c.276A= ENSP00000346969.4:p.Leu92=
ENST00000394971.7:c.480A= ENSP00000378422.3:p.Leu160=
ENST00000394975.2:c.386A= ENSP00000378426.2:p.Tyr129=
ENST00000420057.2:c.348A=
ENST00000472468.1:c.71A= ENSP00000458994.1:p.Tyr24=
ENST00000498155.1:c.483A= ENSP00000417662.1:p.Leu161=
ENST00000529564.1:c.283+2072A= ENSP00000431371.1:n.283+2072A=
ENST00000532364.1:c.173+3317A= ENSP00000460316.1:n.173+3317A=
ENST00000533518.5:c.259A=
NM_001311311.1:c.470A= NP_001298240.1:p.Tyr157=
NM_024006.4:c.386A= NP_076869.1:p.Tyr129=
NM_024006.5:c.386A= NP_076869.1:p.Tyr129=
NM_206824.1:c.276A= NP_996560.1:p.Leu92=
NM_206824.2:c.276A= NP_996560.1:p.Leu92=
XM_011545944.1:c.386A= XP_011544246.1:p.Tyr129=
XM_011545945.1:c.276A= XP_011544247.1:p.Leu92=
XR_950848.1:n.1174A=
NM_024006.6:c.386A= MANE Select NP_076869.1:p.Tyr129=
NM_001311311.2:c.470A= NP_001298240.1:p.Tyr157=
NM_206824.3:c.276A= NP_996560.1:p.Leu92=