Canonical Allele Identifier: CA2245514000
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780854_6780858delinsTGATA , CM000679.2:g.6780854_6780858delinsTGATA GRCh38
NC_000017.10:g.6684173_6684177delinsTGATA , CM000679.1:g.6684173_6684177delinsTGATA GRCh37
NC_000017.9:g.6624897_6624901delinsTGATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.986_990delinsTGATA MANE Select ENSP00000321386.4:p.Leu329=
ENST00000321535.4:c.986_990delinsTGATA ENSP00000321386.4:p.Leu329=
NM_153230.2:c.986_990delinsTGATA NP_694962.1:p.Leu329=
XM_011523697.1:c.986_990delinsTGATA XP_011521999.1:p.Leu329=
XR_243544.3:n.1164_1168delinsTGATA
NM_153230.3:c.986_990delinsTGATA MANE Select NP_694962.1:p.Leu329=
Search 100 bp 5'
Search 100 bp 3'