Canonical Allele Identifier: CA2216889333
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091343C= , CM000678.2:g.31091343C= GRCh38
NC_000016.9:g.31102664C= , CM000678.1:g.31102664C= GRCh37
NC_000016.8:g.31010165C= NCBI36
NG_011564.1:g.8613G=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.284-1G= MANE Select ENSP00000378426.2:n.284-1G=
ENST00000300851.10:c.345-1G= ENSP00000300851.6:n.345-1G=
ENST00000319788.11:c.366-1G= ENSP00000326135.7:n.366-1G=
ENST00000354895.4:c.174-1G= ENSP00000346969.4:n.174-1G=
ENST00000394971.7:c.378-1G= ENSP00000378422.3:n.378-1G=
ENST00000394975.2:c.284-1G= ENSP00000378426.2:n.284-1G=
ENST00000420057.2:c.246-1G=
ENST00000472468.1:c.-32-1G= ENSP00000458994.1:n.-32-1G=
ENST00000498155.1:c.381-1G= ENSP00000417662.1:n.381-1G=
ENST00000529564.1:c.283+1969G= ENSP00000431371.1:n.283+1969G=
ENST00000532364.1:c.173+3214G= ENSP00000460316.1:n.173+3214G=
ENST00000533518.5:c.157-1G=
NM_001311311.1:c.368-1G= NP_001298240.1:n.368-1G=
NM_024006.4:c.284-1G= NP_076869.1:n.284-1G=
NM_024006.5:c.284-1G= NP_076869.1:n.284-1G=
NM_206824.1:c.174-1G= NP_996560.1:n.174-1G=
NM_206824.2:c.174-1G= NP_996560.1:n.174-1G=
XM_011545944.1:c.284-1G= XP_011544246.1:n.284-1G=
XM_011545945.1:c.174-1G= XP_011544247.1:n.174-1G=
XR_950848.1:n.1072-1G=
NM_024006.6:c.284-1G= MANE Select NP_076869.1:n.284-1G=
NM_001311311.2:c.368-1G= NP_001298240.1:n.368-1G=
NM_206824.3:c.174-1G= NP_996560.1:n.174-1G=