HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863424del , CM000672.2:g.87863424del | GRCh38 |
NC_000010.10:g.89623181del , CM000672.1:g.89623181del | GRCh37 |
NC_000010.9:g.89613161del | NCBI36 |
NG_007466.2:g.4987del , LRG_311:g.4987del | |
NG_033079.1:g.5018del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+782del (PTEN) | ENSP00000516674.1:n.-17+782del | |
ENST00000688308.1:c.-17+311del (PTEN) | ENSP00000508752.1:n.-17+311del | |
ENST00000445946.5:c.-933del (KLLN) MANE Select | ENSP00000392204.2:n.-933del | |
ENST00000371953.7:c.-1046del (PTEN) | ENSP00000361021.3:n.-1046del | |
ENST00000445946.3:c.-933del (KLLN) | ENSP00000392204.2:n.-933del | |
NM_001126049.1:c.-933del (KLLN) | NP_001119521.1:n.-933del | |
NM_001126049.2:c.-933del (KLLN) MANE Select | NP_001119521.1:n.-933del |