Linked Data
dbSNP Id:
rs786203981
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863330dup , CM000672.2:g.87863330dup | GRCh38 |
| NC_000010.10:g.89623087dup , CM000672.1:g.89623087dup | GRCh37 |
| NC_000010.9:g.89613067dup | NCBI36 |
| NG_007466.2:g.4893dup , LRG_311:g.4893dup | |
| NG_033079.1:g.5111dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-17+688dup (PTEN) | ENSP00000516674.1:n.-17+688dup | |
| ENST00000688308.1:c.-17+217dup (PTEN) | ENSP00000508752.1:n.-17+217dup | |
| ENST00000445946.5:c.-840dup (KLLN) MANE Select | ENSP00000392204.2:n.-840dup | |
| ENST00000371953.7:c.-1140dup (PTEN) | ENSP00000361021.3:n.-1140dup | |
| ENST00000445946.3:c.-840dup (KLLN) | ENSP00000392204.2:n.-840dup | |
| NM_001126049.1:c.-840dup (KLLN) | NP_001119521.1:n.-840dup | |
| NM_001126049.2:c.-840dup (KLLN) MANE Select | NP_001119521.1:n.-840dup |