Canonical Allele Identifier: CA2632822864
Gene: VKORC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31093749del , CM000678.2:g.31093749del GRCh38
NC_000016.9:g.31105070del , CM000678.1:g.31105070del GRCh37
NC_000016.8:g.31012571del NCBI36
NG_011564.1:g.6209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394975.3:c.174-326del MANE Select ENSP00000378426.2:n.174-326del
ENST00000300851.10:c.174-265del ENSP00000300851.6:n.174-265del
ENST00000319788.11:c.174-326del ENSP00000326135.7:n.174-326del
ENST00000354895.4:c.173+810del ENSP00000346969.4:n.173+810del
ENST00000394971.7:c.268-326del ENSP00000378422.3:n.268-326del
ENST00000394975.2:c.174-326del ENSP00000378426.2:n.174-326del
ENST00000420057.2:c.245+1642del
ENST00000498155.1:c.271-326del ENSP00000417662.1:n.271-326del
ENST00000529564.1:c.174-326del ENSP00000431371.1:n.174-326del
ENST00000532364.1:c.173+810del ENSP00000460316.1:n.173+810del
ENST00000533518.5:c.47-326del
NM_001311311.1:c.174-326del NP_001298240.1:n.174-326del
NM_024006.4:c.174-326del NP_076869.1:n.174-326del
NM_024006.5:c.174-326del NP_076869.1:n.174-326del
NM_206824.1:c.173+810del NP_996560.1:n.173+810del
NM_206824.2:c.173+810del NP_996560.1:n.173+810del
XM_011545944.1:c.174-326del XP_011544246.1:n.174-326del
XM_011545945.1:c.173+810del XP_011544247.1:n.173+810del
XR_950848.1:n.962-326del
NM_024006.6:c.174-326del MANE Select NP_076869.1:n.174-326del
NM_001311311.2:c.174-326del NP_001298240.1:n.174-326del
NM_206824.3:c.173+810del NP_996560.1:n.173+810del