Canonical Allele Identifier: CA2216888973
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091153C= , CM000678.2:g.31091153C= GRCh38
NC_000016.9:g.31102474C= , CM000678.1:g.31102474C= GRCh37
NC_000016.8:g.31009975C= NCBI36
NG_011564.1:g.8803G=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.473G= MANE Select ENSP00000378426.2:p.Gly158=
ENST00000300851.10:c.*84G= ENSP00000300851.6:n.*84G=
ENST00000319788.11:c.*84G= ENSP00000326135.7:n.*84G=
ENST00000354895.4:c.*84G= ENSP00000346969.4:n.*84G=
ENST00000394971.7:c.*84G= ENSP00000378422.3:n.*84G=
ENST00000394975.2:c.473G= ENSP00000378426.2:p.Gly158=
ENST00000420057.2:c.435G=
ENST00000529564.1:c.283+2159G= ENSP00000431371.1:n.283+2159G=
ENST00000532364.1:c.173+3404G= ENSP00000460316.1:n.173+3404G=
ENST00000533518.5:c.346G=
NM_001311311.1:c.557G= NP_001298240.1:p.Gly186=
NM_024006.4:c.473G= NP_076869.1:p.Gly158=
NM_024006.5:c.473G= NP_076869.1:p.Gly158=
NM_206824.1:c.*84G= NP_996560.1:n.*84G=
NM_206824.2:c.*84G= NP_996560.1:n.*84G=
XM_011545944.1:c.473G= XP_011544246.1:p.Gly158=
XM_011545945.1:c.*84G= XP_011544247.1:n.*84G=
XR_950848.1:n.1261G=
NM_024006.6:c.473G= MANE Select NP_076869.1:p.Gly158=
NM_001311311.2:c.557G= NP_001298240.1:p.Gly186=
NM_206824.3:c.*84G= NP_996560.1:n.*84G=