Canonical Allele Identifier: CA2808354314
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780465_6780466del , CM000679.2:g.6780465_6780466del GRCh38
NC_000017.10:g.6683784_6683785del , CM000679.1:g.6683784_6683785del GRCh37
NC_000017.9:g.6624508_6624509del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.597_598del MANE Select ENSP00000321386.4:p.Ile200ArgfsTer?
ENST00000321535.4:c.597_598del ENSP00000321386.4:p.Ile200ArgfsTer?
NM_153230.2:c.597_598del NP_694962.1:p.Ile200ArgfsTer?
XM_011523697.1:c.597_598del XP_011521999.1:p.Ile200ArgfsTer?
XR_243544.3:n.775_776del
NM_153230.3:c.597_598del MANE Select NP_694962.1:p.Ile200ArgfsTer?