Canonical Allele Identifier: CA2635734290
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780524-C-CCA
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780525_6780526dup , CM000679.2:g.6780525_6780526dup GRCh38
NC_000017.10:g.6683844_6683845dup , CM000679.1:g.6683844_6683845dup GRCh37
NC_000017.9:g.6624568_6624569dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.657_658dup MANE Select ENSP00000321386.4:p.Met220ThrfsTer11
ENST00000321535.4:c.657_658dup ENSP00000321386.4:p.Met220ThrfsTer11
NM_153230.2:c.657_658dup NP_694962.1:p.Met220ThrfsTer11
XM_011523697.1:c.657_658dup XP_011521999.1:p.Met220ThrfsTer11
XR_243544.3:n.835_836dup
NM_153230.3:c.657_658dup MANE Select NP_694962.1:p.Met220ThrfsTer11
Search 100 bp 5'
Search 100 bp 3'