Canonical Allele Identifier: CA8332497
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs770602614
ExAC: 17:6684044 ACTT / A
gnomAD v2: 17-6684044-ACTT-A
gnomAD v3: 17-6780725-ACTT-A
gnomAD v4: 17-6780725-ACTT-A
MyVariant Identifiers: chr17:g.6684045_6684047del (hg19) chr17:g.6780726_6780728del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780732_6780734del , CM000679.2:g.6780732_6780734del GRCh38
NC_000017.10:g.6684051_6684053del , CM000679.1:g.6684051_6684053del GRCh37
NC_000017.9:g.6624775_6624777del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.864_866del MANE Select ENSP00000321386.4:p.Phe289del
ENST00000321535.4:c.864_866del ENSP00000321386.4:p.Phe289del
NM_153230.2:c.864_866del NP_694962.1:p.Phe289del
XM_011523697.1:c.864_866del XP_011521999.1:p.Phe289del
XR_243544.3:n.1042_1044del
NM_153230.3:c.864_866del MANE Select NP_694962.1:p.Phe289del
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