Canonical Allele Identifier: CA2843013876
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31091052T>A , CM000678.2:g.31091052T>A GRCh38
NC_000016.9:g.31102373T>A , CM000678.1:g.31102373T>A GRCh37
NC_000016.8:g.31009874T>A NCBI36
NG_011564.1:g.8904A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.*82A>T MANE Select ENSP00000378426.2:n.*82A>T
ENST00000300851.10:c.*185A>T ENSP00000300851.6:n.*185A>T
ENST00000319788.11:c.*185A>T ENSP00000326135.7:n.*185A>T
ENST00000354895.4:c.*185A>T ENSP00000346969.4:n.*185A>T
ENST00000394975.2:c.*82A>T ENSP00000378426.2:n.*82A>T
ENST00000420057.2:c.536A>T
ENST00000529564.1:c.283+2260A>T ENSP00000431371.1:n.283+2260A>T
ENST00000532364.1:c.173+3505A>T ENSP00000460316.1:n.173+3505A>T
ENST00000533518.5:c.407+40A>T
NM_001311311.1:c.*82A>T NP_001298240.1:n.*82A>T
NM_024006.4:c.*82A>T NP_076869.1:n.*82A>T
NM_024006.5:c.*82A>T NP_076869.1:n.*82A>T
NM_206824.1:c.*185A>T NP_996560.1:n.*185A>T
NM_206824.2:c.*185A>T NP_996560.1:n.*185A>T
XM_011545944.1:c.*82A>T XP_011544246.1:n.*82A>T
XM_011545945.1:c.*185A>T XP_011544247.1:n.*185A>T
XR_950848.1:n.1362A>T
NM_024006.6:c.*82A>T MANE Select NP_076869.1:n.*82A>T
NM_001311311.2:c.*82A>T NP_001298240.1:n.*82A>T
NM_206824.3:c.*185A>T NP_996560.1:n.*185A>T