APPRIS principal isoforms and MANE Select transcripts in clinical variant interpretation
Fernando Campo del PozoiD, José Manuel Rodrı́gueziD, Jesús VázqueziD, Michael L. TressiD
Abstract
Most coding genes are able to generate multiple alternatively spliced transcripts. Determining which of these transcript variants produces the main protein isoform, and which of a genes multiple splice variants are functionally important, is crucial in comparative genomics and essential for clinical variant interpretation. Here we show that the principal isoforms chosen by APPRIS and the MANE Select variants provide the best approximations of the main cellular protein isoforms. Principal isoforms are predicted from conservation and from protein features, and MANE transcripts are chosen from the consensus between teams of expert manual curators. APPRIS principal isoforms coincide in over 94% of coding genes with MANE Select transcripts and the two methods are particularly discriminating when they agree on the main splice variant. Where the two methods agree, the splice variants coincide with the main isoform detected in proteomics experiments in 98.2% of genes with multiple protein isoforms. We also find that almost all ClinVar pathogenic mutations map to MANE Select or APPRIS principal isoforms. Where APPRIS and MANE agree on the main isoform, 99.93% of validated pathogenic variants map to principal rather than alternative exons. MANE Plus Clinical transcripts cover most validated pathogenic mutations in alternative coding exons. TRIFID functional importance scores are particularly useful for distinguishing clinically important alternative isoforms: the highest scoring TRIFID isoforms are more than 300 times more likely to have validated pathogenic mutations. We find that APPRIS, MANE and TRIFID are important for determining the biological relevance of splice isoforms and should be an essential part of clinical variant interpretation.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Disease-associated genetic variants can cause mutations in tissue-specific protein isoforms
Giovanna Weykopf, Mihaly Badonyi, … Simon Cameron Biddie·bioRxiv·Jul 24, 2025
- Investigating the pathogenicity of missense spliceogenic variants using whole-genome sequencing, RNA-sequencing, and proteomics data from population and clinical research cohorts
Mwenda R. Rintari, V. Kartik Chundru, … Caroline Fiona Wright·medRxiv·Oct 13, 2026
- S-CAP extends clinical-grade pathogenicity prediction to genetic variants that affect RNA splicing
Karthik A. Jagadeesh, Joseph M. Paggi, … Gill Bejerano·Nature GeneticsPeer-reviewed·Feb 25, 2019
- MetaSplice: pathogenicity prediction and ACMG/AMP evidence for intronic variants outside the canonical splice sites
Xiaoming Liu·bioRxiv·Jul 27, 2026
- Curating clinically relevant transcripts for the interpretation of sequence variants
Marina T. DiStefano, Sarah E. Hemphill, … Ahmad N. Abou Tayoun·Journal of Molecular DiagnosticsPeer-reviewed·Aug 7, 2018
- Widespread naturally variable human exons aid genetic interpretation
Hannah N. Jacobs, Bram L. Gorissen, … Christopher B. Burge·Nature CommunicationsPeer-reviewed·Dec 16, 2025