Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863379T>C , CM000672.2:g.87863379T>C | GRCh38 |
| NC_000010.10:g.89623136T>C , CM000672.1:g.89623136T>C | GRCh37 |
| NC_000010.9:g.89613116T>C | NCBI36 |
| NG_007466.2:g.4942T>C , LRG_311:g.4942T>C | |
| NG_033079.1:g.5059A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-17+737T>C (PTEN) | ENSP00000516674.1:n.-17+737T>C | |
| ENST00000688308.1:c.-17+266T>C (PTEN) | ENSP00000508752.1:n.-17+266T>C | |
| ENST00000445946.5:c.-892A>G (KLLN) MANE Select | ENSP00000392204.2:n.-892A>G | |
| ENST00000371953.7:c.-1091T>C (PTEN) | ENSP00000361021.3:n.-1091T>C | |
| ENST00000445946.3:c.-892A>G (KLLN) | ENSP00000392204.2:n.-892A>G | |
| NM_001126049.1:c.-892A>G (KLLN) | NP_001119521.1:n.-892A>G | |
| NM_001126049.2:c.-892A>G (KLLN) MANE Select | NP_001119521.1:n.-892A>G |