Canonical Allele Identifier: CA2808354315
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780640_6780642del , CM000679.2:g.6780640_6780642del GRCh38
NC_000017.10:g.6683959_6683961del , CM000679.1:g.6683959_6683961del GRCh37
NC_000017.9:g.6624683_6624685del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.772_774del MANE Select ENSP00000321386.4:p.Cys258del
ENST00000321535.4:c.772_774del ENSP00000321386.4:p.Cys258del
NM_153230.2:c.772_774del NP_694962.1:p.Cys258del
XM_011523697.1:c.772_774del XP_011521999.1:p.Cys258del
XR_243544.3:n.950_952del
NM_153230.3:c.772_774del MANE Select NP_694962.1:p.Cys258del
Search 100 bp 5'
Search 100 bp 3'