HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863013_87863028del , CM000672.2:g.87863013_87863028del | GRCh38 |
NC_000010.10:g.89622770_89622785del , CM000672.1:g.89622770_89622785del | GRCh37 |
NC_000010.9:g.89612750_89612765del | NCBI36 |
NG_007466.2:g.4576_4591del , LRG_311:g.4576_4591del | |
NG_033079.1:g.5413_5428del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+371_-17+386del (PTEN) | ENSP00000516674.1:n.-17+371_-17+386del | |
ENST00000688308.1:c.-117_-102del (PTEN) | ENSP00000508752.1:n.-117_-102del | |
ENST00000445946.5:c.-538_-523del (KLLN) MANE Select | ENSP00000392204.2:n.-538_-523del | |
ENST00000445946.3:c.-538_-523del (KLLN) | ENSP00000392204.2:n.-538_-523del | |
NM_001126049.1:c.-538_-523del (KLLN) | NP_001119521.1:n.-538_-523del | |
NM_001126049.2:c.-538_-523del (KLLN) MANE Select | NP_001119521.1:n.-538_-523del |