Canonical Allele Identifier: CA2216893980
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31094573G= , CM000678.2:g.31094573G= GRCh38
NC_000016.9:g.31105894G= , CM000678.1:g.31105894G= GRCh37
NC_000016.8:g.31013395G= NCBI36
NG_011564.1:g.5383C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.157C= MANE Select ENSP00000378426.2:p.Arg53=
ENST00000300851.10:c.157C= ENSP00000300851.6:p.Arg53=
ENST00000319788.11:c.157C= ENSP00000326135.7:p.Arg53=
ENST00000354895.4:c.157C= ENSP00000346969.4:p.Arg53=
ENST00000394975.2:c.157C= ENSP00000378426.2:p.Arg53=
ENST00000420057.2:c.245+816C=
ENST00000498155.1:c.270+816C= ENSP00000417662.1:n.270+816C=
ENST00000529564.1:c.157C= ENSP00000431371.1:p.Arg53=
ENST00000532364.1:c.157C= ENSP00000460316.1:p.Arg53=
ENST00000533518.5:c.30C=
NM_001311311.1:c.157C= NP_001298240.1:p.Arg53=
NM_024006.4:c.157C= NP_076869.1:p.Arg53=
NM_024006.5:c.157C= NP_076869.1:p.Arg53=
NM_206824.1:c.157C= NP_996560.1:p.Arg53=
NM_206824.2:c.157C= NP_996560.1:p.Arg53=
XM_011545944.1:c.157C= XP_011544246.1:p.Arg53=
XM_011545945.1:c.157C= XP_011544247.1:p.Arg53=
XR_950848.1:n.945C=
NM_024006.6:c.157C= MANE Select NP_076869.1:p.Arg53=
NM_001311311.2:c.157C= NP_001298240.1:p.Arg53=
NM_206824.3:c.157C= NP_996560.1:p.Arg53=