Canonical Allele Identifier: CA2635734663
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780758-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780758_6780759insA , CM000679.2:g.6780758_6780759insA GRCh38
NC_000017.10:g.6684077_6684078insA , CM000679.1:g.6684077_6684078insA GRCh37
NC_000017.9:g.6624801_6624802insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.890_891insA MANE Select ENSP00000321386.4:p.Ala299GlyfsTer22
ENST00000321535.4:c.890_891insA ENSP00000321386.4:p.Ala299GlyfsTer22
NM_153230.2:c.890_891insA NP_694962.1:p.Ala299GlyfsTer22
XM_011523697.1:c.890_891insA XP_011521999.1:p.Ala299GlyfsTer22
XR_243544.3:n.1068_1069insA
NM_153230.3:c.890_891insA MANE Select NP_694962.1:p.Ala299GlyfsTer22
Search 100 bp 5'
Search 100 bp 3'