I'm working with variants which were aligned against an older genome (hg19) and, thus,annotated using an older Ensembl release (75). Would it still make sense to use APPRIS to determine the principal isoform for each coding variant? Are Ensembl IDs stable across releases (in the sense that a particular transcript ID always refers to the same set of exons)?
Thanks Denise,
Do you think the principal transcripts in APPRIS would still exist in e.g. Ensembl release 54?
I believe there were fewer spliced isoforms annotated back them in NCBI36. If I take one example BRCA2 I can see that we now have 7 transcripts and back then we had 1. For DMD, there were 15 isoforms in 2009 and 30 transcripts now. The stable IDs then and now should be the same. So what is annotated as PIs now can be traced back to the annotation of NCBI36. APPRIS was originally developed using Ensembl release 56. Would it be worth contacting APPRIS developers? Failing having APPRIS for Ensembl release 54, I'd focus on the transcripts that have got CCDS and failed that I'd focus on those resulting from the merged set between Ensembl and HAVANA.