HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863045_87863047del , CM000672.2:g.87863045_87863047del | GRCh38 |
NC_000010.10:g.89622802_89622804del , CM000672.1:g.89622802_89622804del | GRCh37 |
NC_000010.9:g.89612782_89612784del | NCBI36 |
NG_007466.2:g.4608_4610del , LRG_311:g.4608_4610del | |
NG_033079.1:g.5391_5393del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+403_-17+405del (PTEN) | ENSP00000516674.1:n.-17+403_-17+405del | |
ENST00000688308.1:c.-85_-83del (PTEN) | ENSP00000508752.1:n.-85_-83del | |
ENST00000445946.5:c.-560_-558del (KLLN) MANE Select | ENSP00000392204.2:n.-560_-558del | |
ENST00000445946.3:c.-560_-558del (KLLN) | ENSP00000392204.2:n.-560_-558del | |
NM_001126049.1:c.-560_-558del (KLLN) | NP_001119521.1:n.-560_-558del | |
NM_001126049.2:c.-560_-558del (KLLN) MANE Select | NP_001119521.1:n.-560_-558del |