Canonical Allele Identifier: CA2245513806
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780725_6780728delinsACTT , CM000679.2:g.6780725_6780728delinsACTT GRCh38
NC_000017.10:g.6684044_6684047delinsACTT , CM000679.1:g.6684044_6684047delinsACTT GRCh37
NC_000017.9:g.6624768_6624771delinsACTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.857_860delinsACTT MANE Select ENSP00000321386.4:p.Asn286=
ENST00000321535.4:c.857_860delinsACTT ENSP00000321386.4:p.Asn286=
NM_153230.2:c.857_860delinsACTT NP_694962.1:p.Asn286=
XM_011523697.1:c.857_860delinsACTT XP_011521999.1:p.Asn286=
XR_243544.3:n.1035_1038delinsACTT
NM_153230.3:c.857_860delinsACTT MANE Select NP_694962.1:p.Asn286=
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