HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863154del , CM000672.2:g.87863154del | GRCh38 |
NC_000010.10:g.89622911del , CM000672.1:g.89622911del | GRCh37 |
NC_000010.9:g.89612891del | NCBI36 |
NG_007466.2:g.4717del , LRG_311:g.4717del | |
NG_033079.1:g.5286del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+512del (PTEN) | ENSP00000516674.1:n.-17+512del | |
ENST00000688308.1:c.-17+41del (PTEN) | ENSP00000508752.1:n.-17+41del | |
ENST00000445946.5:c.-665del (KLLN) MANE Select | ENSP00000392204.2:n.-665del | |
ENST00000371953.7:c.-1316del (PTEN) | ENSP00000361021.3:n.-1316del | |
ENST00000445946.3:c.-665del (KLLN) | ENSP00000392204.2:n.-665del | |
NM_001126049.1:c.-665del (KLLN) | NP_001119521.1:n.-665del | |
NM_001126049.2:c.-665del (KLLN) MANE Select | NP_001119521.1:n.-665del |