Canonical Allele Identifier: CA2216888555
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31090927C= , CM000678.2:g.31090927C= GRCh38
NC_000016.9:g.31102248C= , CM000678.1:g.31102248C= GRCh37
NC_000016.8:g.31009749C= NCBI36
NG_011564.1:g.9029G=

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.*207G= MANE Select ENSP00000378426.2:n.*207G=
ENST00000300851.10:c.*310G= ENSP00000300851.6:n.*310G=
ENST00000319788.11:c.*310G= ENSP00000326135.7:n.*310G=
ENST00000354895.4:c.*310G= ENSP00000346969.4:n.*310G=
ENST00000394975.2:c.*207G= ENSP00000378426.2:n.*207G=
ENST00000420057.2:c.661G=
ENST00000529564.1:c.283+2385G= ENSP00000431371.1:n.283+2385G=
ENST00000532364.1:c.173+3630G= ENSP00000460316.1:n.173+3630G=
ENST00000533518.5:c.407+165G=
NM_001311311.1:c.*207G= NP_001298240.1:n.*207G=
NM_024006.4:c.*207G= NP_076869.1:n.*207G=
NM_024006.5:c.*207G= NP_076869.1:n.*207G=
NM_206824.1:c.*310G= NP_996560.1:n.*310G=
NM_206824.2:c.*310G= NP_996560.1:n.*310G=
XM_011545944.1:c.*207G= XP_011544246.1:n.*207G=
XM_011545945.1:c.*310G= XP_011544247.1:n.*310G=
XR_950848.1:n.1487G=
NM_024006.6:c.*207G= MANE Select NP_076869.1:n.*207G=
NM_001311311.2:c.*207G= NP_001298240.1:n.*207G=
NM_206824.3:c.*310G= NP_996560.1:n.*310G=