Canonical Allele Identifier: CA2245513944
Gene: FBXO39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780811_6780814delinsAGCT , CM000679.2:g.6780811_6780814delinsAGCT GRCh38
NC_000017.10:g.6684130_6684133delinsAGCT , CM000679.1:g.6684130_6684133delinsAGCT GRCh37
NC_000017.9:g.6624854_6624857delinsAGCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.943_946delinsAGCT MANE Select ENSP00000321386.4:p.Ser315=
ENST00000321535.4:c.943_946delinsAGCT ENSP00000321386.4:p.Ser315=
NM_153230.2:c.943_946delinsAGCT NP_694962.1:p.Ser315=
XM_011523697.1:c.943_946delinsAGCT XP_011521999.1:p.Ser315=
XR_243544.3:n.1121_1124delinsAGCT
NM_153230.3:c.943_946delinsAGCT MANE Select NP_694962.1:p.Ser315=
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Search 100 bp 3'