Canonical Allele Identifier: CA2216889139
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091256G= , CM000678.2:g.31091256G= GRCh38
NC_000016.9:g.31102577G= , CM000678.1:g.31102577G= GRCh37
NC_000016.8:g.31010078G= NCBI36
NG_011564.1:g.8700C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.370C= MANE Select ENSP00000378426.2:p.Leu124=
ENST00000300851.10:c.431C= ENSP00000300851.6:p.Pro144=
ENST00000319788.11:c.452C= ENSP00000326135.7:p.Pro151=
ENST00000354895.4:c.260C= ENSP00000346969.4:p.Pro87=
ENST00000394971.7:c.464C= ENSP00000378422.3:p.Pro155=
ENST00000394975.2:c.370C= ENSP00000378426.2:p.Leu124=
ENST00000420057.2:c.332C=
ENST00000472468.1:c.55C= ENSP00000458994.1:p.Leu19=
ENST00000498155.1:c.467C= ENSP00000417662.1:p.Pro156=
ENST00000529564.1:c.283+2056C= ENSP00000431371.1:n.283+2056C=
ENST00000532364.1:c.173+3301C= ENSP00000460316.1:n.173+3301C=
ENST00000533518.5:c.243C=
NM_001311311.1:c.454C= NP_001298240.1:p.Leu152=
NM_024006.4:c.370C= NP_076869.1:p.Leu124=
NM_024006.5:c.370C= NP_076869.1:p.Leu124=
NM_206824.1:c.260C= NP_996560.1:p.Pro87=
NM_206824.2:c.260C= NP_996560.1:p.Pro87=
XM_011545944.1:c.370C= XP_011544246.1:p.Leu124=
XM_011545945.1:c.260C= XP_011544247.1:p.Pro87=
XR_950848.1:n.1158C=
NM_024006.6:c.370C= MANE Select NP_076869.1:p.Leu124=
NM_001311311.2:c.454C= NP_001298240.1:p.Leu152=
NM_206824.3:c.260C= NP_996560.1:p.Pro87=