Canonical Allele Identifier: CA2216888743
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091014G= , CM000678.2:g.31091014G= GRCh38
NC_000016.9:g.31102335G= , CM000678.1:g.31102335G= GRCh37
NC_000016.8:g.31009836G= NCBI36
NG_011564.1:g.8942C=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*120C= MANE Select ENSP00000378426.2:n.*120C=
ENST00000300851.10:c.*223C= ENSP00000300851.6:n.*223C=
ENST00000319788.11:c.*223C= ENSP00000326135.7:n.*223C=
ENST00000354895.4:c.*223C= ENSP00000346969.4:n.*223C=
ENST00000394975.2:c.*120C= ENSP00000378426.2:n.*120C=
ENST00000420057.2:c.574C=
ENST00000529564.1:c.283+2298C= ENSP00000431371.1:n.283+2298C=
ENST00000532364.1:c.173+3543C= ENSP00000460316.1:n.173+3543C=
ENST00000533518.5:c.407+78C=
NM_001311311.1:c.*120C= NP_001298240.1:n.*120C=
NM_024006.4:c.*120C= NP_076869.1:n.*120C=
NM_024006.5:c.*120C= NP_076869.1:n.*120C=
NM_206824.1:c.*223C= NP_996560.1:n.*223C=
NM_206824.2:c.*223C= NP_996560.1:n.*223C=
XM_011545944.1:c.*120C= XP_011544246.1:n.*120C=
XM_011545945.1:c.*223C= XP_011544247.1:n.*223C=
XR_950848.1:n.1400C=
NM_024006.6:c.*120C= MANE Select NP_076869.1:n.*120C=
NM_001311311.2:c.*120C= NP_001298240.1:n.*120C=
NM_206824.3:c.*223C= NP_996560.1:n.*223C=