Canonical Allele Identifier: CA2576144626
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780732_6780734dup , CM000679.2:g.6780732_6780734dup GRCh38
NC_000017.10:g.6684051_6684053dup , CM000679.1:g.6684051_6684053dup GRCh37
NC_000017.9:g.6624775_6624777dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.864_866dup MANE Select ENSP00000321386.4:p.Phe289_Glu290insPhe
ENST00000321535.4:c.864_866dup ENSP00000321386.4:p.Phe289_Glu290insPhe
NM_153230.2:c.864_866dup NP_694962.1:p.Phe289_Glu290insPhe
XM_011523697.1:c.864_866dup XP_011521999.1:p.Phe289_Glu290insPhe
XR_243544.3:n.1042_1044dup
NM_153230.3:c.864_866dup MANE Select NP_694962.1:p.Phe289_Glu290insPhe
Search 100 bp 5'
Search 100 bp 3'