Canonical Allele Identifier: CA2216892150
Gene: VKORC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093557G= , CM000678.2:g.31093557G= GRCh38
NC_000016.9:g.31104878G= , CM000678.1:g.31104878G= GRCh37
NC_000016.8:g.31012379G= NCBI36
NG_011564.1:g.6399C=

Transcript Alleles

HGVS Amino-acid Change
NM_024006.6:c.174-136C= MANE Select NP_076869.1:n.174-136C=
ENST00000394975.3:c.174-136C= MANE Select ENSP00000378426.2:n.174-136C=
NM_001311311.1:c.174-136C= NP_001298240.1:n.174-136C=
NM_001311311.2:c.174-136C= NP_001298240.1:n.174-136C=
NM_024006.4:c.174-136C= NP_076869.1:n.174-136C=
NM_024006.5:c.174-136C= NP_076869.1:n.174-136C=
NM_206824.1:c.173+1000C= NP_996560.1:n.173+1000C=
NM_206824.2:c.173+1000C= NP_996560.1:n.173+1000C=
NM_206824.3:c.173+1000C= NP_996560.1:n.173+1000C=
ENST00000300851.10:c.174-75C= ENSP00000300851.6:n.174-75C=
ENST00000319788.11:c.174-136C= ENSP00000326135.7:n.174-136C=
ENST00000354895.4:c.173+1000C= ENSP00000346969.4:n.173+1000C=
ENST00000394971.7:c.268-136C= ENSP00000378422.3:n.268-136C=
ENST00000394975.2:c.174-136C= ENSP00000378426.2:n.174-136C=
ENST00000420057.2:c.245+1832C=
ENST00000472468.1:c.-278C= ENSP00000458994.1:n.-278C=
ENST00000498155.1:c.271-136C= ENSP00000417662.1:n.271-136C=
ENST00000529564.1:c.174-136C= ENSP00000431371.1:n.174-136C=
ENST00000532364.1:c.173+1000C= ENSP00000460316.1:n.173+1000C=
ENST00000533518.5:c.47-136C=
XM_011545944.1:c.174-136C= XP_011544246.1:n.174-136C=
XM_011545945.1:c.173+1000C= XP_011544247.1:n.173+1000C=
XR_950848.1:n.962-136C=