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NPM1::FGF18

Known partner

Canonical-transcript structure of the two partner genes, and the read-level evidence supporting the fusion in each tumor sample.

Known studies

No published studies in the Mitelman database describe the NPM1::FGF18 gene fusion. It may be novel, private to this case, or a technical artifact — absence from a curated database is not by itself evidence either way.

Canonical transcripts in genomic order spliced together in the fusion mRNA 8.7 kb apart chr5 NPM1 (+) ENST00000296930 · Ensembl canonical 171,388,006 breakpoint 171,387,849 171,410,900 11 exons · 23.1 kb chr5 FGF18 (+) ENST00000274625 · Ensembl canonical 171,436,093 breakpoint 171,419,647 171,457,626 5 exons · 38.0 kb
Canonical transcripts shown in genomic order on chr5 (lower-coordinate gene on the left). Each gene is drawn at its own zoom level. Introns are compressed to 1% of their genomic length so the exons are easier to see — the pixel-space x-axis is therefore non-linear, but the labelled start and end coordinates of each transcript are exact. The gap shown between the two panels (when on the same chromosome) is the actual distance between gene bodies. Transcript IDs are MANE Select where available, else Ensembl_canonical, else the longest protein-coding transcript.

Left hand (primary)

Reportable 2 fragments (1 split, 1 discordant) · NPM1 exon 1 → FGF18 exon 3

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