Canonical Allele Identifier: CA2245513745
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780682_6780683delinsTC , CM000679.2:g.6780682_6780683delinsTC GRCh38
NC_000017.10:g.6684001_6684002delinsTC , CM000679.1:g.6684001_6684002delinsTC GRCh37
NC_000017.9:g.6624725_6624726delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.814_815delinsTC MANE Select ENSP00000321386.4:p.Ser272=
ENST00000321535.4:c.814_815delinsTC ENSP00000321386.4:p.Ser272=
NM_153230.2:c.814_815delinsTC NP_694962.1:p.Ser272=
XM_011523697.1:c.814_815delinsTC XP_011521999.1:p.Ser272=
XR_243544.3:n.992_993delinsTC
NM_153230.3:c.814_815delinsTC MANE Select NP_694962.1:p.Ser272=
Search 100 bp 5'
Search 100 bp 3'