Canonical Allele Identifier: CA2216888755
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091019G= , CM000678.2:g.31091019G= GRCh38
NC_000016.9:g.31102340G= , CM000678.1:g.31102340G= GRCh37
NC_000016.8:g.31009841G= NCBI36
NG_011564.1:g.8937C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*115C= MANE Select ENSP00000378426.2:n.*115C=
ENST00000300851.10:c.*218C= ENSP00000300851.6:n.*218C=
ENST00000319788.11:c.*218C= ENSP00000326135.7:n.*218C=
ENST00000354895.4:c.*218C= ENSP00000346969.4:n.*218C=
ENST00000394975.2:c.*115C= ENSP00000378426.2:n.*115C=
ENST00000420057.2:c.569C=
ENST00000529564.1:c.283+2293C= ENSP00000431371.1:n.283+2293C=
ENST00000532364.1:c.173+3538C= ENSP00000460316.1:n.173+3538C=
ENST00000533518.5:c.407+73C=
NM_001311311.1:c.*115C= NP_001298240.1:n.*115C=
NM_024006.4:c.*115C= NP_076869.1:n.*115C=
NM_024006.5:c.*115C= NP_076869.1:n.*115C=
NM_206824.1:c.*218C= NP_996560.1:n.*218C=
NM_206824.2:c.*218C= NP_996560.1:n.*218C=
XM_011545944.1:c.*115C= XP_011544246.1:n.*115C=
XM_011545945.1:c.*218C= XP_011544247.1:n.*218C=
XR_950848.1:n.1395C=
NM_024006.6:c.*115C= MANE Select NP_076869.1:n.*115C=
NM_001311311.2:c.*115C= NP_001298240.1:n.*115C=
NM_206824.3:c.*218C= NP_996560.1:n.*218C=