Canonical Allele Identifier: CA2635734794
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780827-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780830del , CM000679.2:g.6780830del GRCh38
NC_000017.10:g.6684149del , CM000679.1:g.6684149del GRCh37
NC_000017.9:g.6624873del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.962del MANE Select ENSP00000321386.4:p.Pro321GlnfsTer5
ENST00000321535.4:c.962del ENSP00000321386.4:p.Pro321GlnfsTer5
NM_153230.2:c.962del NP_694962.1:p.Pro321GlnfsTer5
XM_011523697.1:c.962del XP_011521999.1:p.Pro321GlnfsTer5
XR_243544.3:n.1140del
NM_153230.3:c.962del MANE Select NP_694962.1:p.Pro321GlnfsTer5
Search 100 bp 5'
Search 100 bp 3'