Canonical Allele Identifier: CA2635734280
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780516-C-CA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780521dup , CM000679.2:g.6780521dup GRCh38
NC_000017.10:g.6683840dup , CM000679.1:g.6683840dup GRCh37
NC_000017.9:g.6624564dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.653dup MANE Select ENSP00000321386.4:p.Thr219AspfsTer24
ENST00000321535.4:c.653dup ENSP00000321386.4:p.Thr219AspfsTer24
NM_153230.2:c.653dup NP_694962.1:p.Thr219AspfsTer24
XM_011523697.1:c.653dup XP_011521999.1:p.Thr219AspfsTer24
XR_243544.3:n.831dup
NM_153230.3:c.653dup MANE Select NP_694962.1:p.Thr219AspfsTer24
Search 100 bp 5'
Search 100 bp 3'