Canonical Allele Identifier: CA2216888727
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091001G= , CM000678.2:g.31091001G= GRCh38
NC_000016.9:g.31102322G= , CM000678.1:g.31102322G= GRCh37
NC_000016.8:g.31009823G= NCBI36
NG_011564.1:g.8955C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*133C= MANE Select ENSP00000378426.2:n.*133C=
ENST00000300851.10:c.*236C= ENSP00000300851.6:n.*236C=
ENST00000319788.11:c.*236C= ENSP00000326135.7:n.*236C=
ENST00000354895.4:c.*236C= ENSP00000346969.4:n.*236C=
ENST00000394975.2:c.*133C= ENSP00000378426.2:n.*133C=
ENST00000420057.2:c.587C=
ENST00000529564.1:c.283+2311C= ENSP00000431371.1:n.283+2311C=
ENST00000532364.1:c.173+3556C= ENSP00000460316.1:n.173+3556C=
ENST00000533518.5:c.407+91C=
NM_001311311.1:c.*133C= NP_001298240.1:n.*133C=
NM_024006.4:c.*133C= NP_076869.1:n.*133C=
NM_024006.5:c.*133C= NP_076869.1:n.*133C=
NM_206824.1:c.*236C= NP_996560.1:n.*236C=
NM_206824.2:c.*236C= NP_996560.1:n.*236C=
XM_011545944.1:c.*133C= XP_011544246.1:n.*133C=
XM_011545945.1:c.*236C= XP_011544247.1:n.*236C=
XR_950848.1:n.1413C=
NM_024006.6:c.*133C= MANE Select NP_076869.1:n.*133C=
NM_001311311.2:c.*133C= NP_001298240.1:n.*133C=
NM_206824.3:c.*236C= NP_996560.1:n.*236C=