Canonical Allele Identifier: CA2245513927
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780798_6780800delinsCAT , CM000679.2:g.6780798_6780800delinsCAT GRCh38
NC_000017.10:g.6684117_6684119delinsCAT , CM000679.1:g.6684117_6684119delinsCAT GRCh37
NC_000017.9:g.6624841_6624843delinsCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.930_932delinsCAT MANE Select ENSP00000321386.4:p.Ser310=
ENST00000321535.4:c.930_932delinsCAT ENSP00000321386.4:p.Ser310=
NM_153230.2:c.930_932delinsCAT NP_694962.1:p.Ser310=
XM_011523697.1:c.930_932delinsCAT XP_011521999.1:p.Ser310=
XR_243544.3:n.1108_1110delinsCAT
NM_153230.3:c.930_932delinsCAT MANE Select NP_694962.1:p.Ser310=
Search 100 bp 5'
Search 100 bp 3'