Canonical Allele Identifier: CA2216888970
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091147G= , CM000678.2:g.31091147G= GRCh38
NC_000016.9:g.31102468G= , CM000678.1:g.31102468G= GRCh37
NC_000016.8:g.31009969G= NCBI36
NG_011564.1:g.8809C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.479C= MANE Select ENSP00000378426.2:p.Ala160=
ENST00000300851.10:c.*90C= ENSP00000300851.6:n.*90C=
ENST00000319788.11:c.*90C= ENSP00000326135.7:n.*90C=
ENST00000354895.4:c.*90C= ENSP00000346969.4:n.*90C=
ENST00000394971.7:c.*90C= ENSP00000378422.3:n.*90C=
ENST00000394975.2:c.479C= ENSP00000378426.2:p.Ala160=
ENST00000420057.2:c.441C=
ENST00000529564.1:c.283+2165C= ENSP00000431371.1:n.283+2165C=
ENST00000532364.1:c.173+3410C= ENSP00000460316.1:n.173+3410C=
ENST00000533518.5:c.352C=
NM_001311311.1:c.563C= NP_001298240.1:p.Ala188=
NM_024006.4:c.479C= NP_076869.1:p.Ala160=
NM_024006.5:c.479C= NP_076869.1:p.Ala160=
NM_206824.1:c.*90C= NP_996560.1:n.*90C=
NM_206824.2:c.*90C= NP_996560.1:n.*90C=
XM_011545944.1:c.479C= XP_011544246.1:p.Ala160=
XM_011545945.1:c.*90C= XP_011544247.1:n.*90C=
XR_950848.1:n.1267C=
NM_024006.6:c.479C= MANE Select NP_076869.1:p.Ala160=
NM_001311311.2:c.563C= NP_001298240.1:p.Ala188=
NM_206824.3:c.*90C= NP_996560.1:n.*90C=