HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863061_87863064del , CM000672.2:g.87863061_87863064del | GRCh38 |
NC_000010.10:g.89622818_89622821del , CM000672.1:g.89622818_89622821del | GRCh37 |
NC_000010.9:g.89612798_89612801del | NCBI36 |
NG_007466.2:g.4624_4627del , LRG_311:g.4624_4627del | |
NG_033079.1:g.5374_5377del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+419_-17+422del (PTEN) | ENSP00000516674.1:n.-17+419_-17+422del | |
ENST00000688308.1:c.-69_-66del (PTEN) | ENSP00000508752.1:n.-69_-66del | |
ENST00000445946.5:c.-577_-574del (KLLN) MANE Select | ENSP00000392204.2:n.-577_-574del | |
ENST00000445946.3:c.-577_-574del (KLLN) | ENSP00000392204.2:n.-577_-574del | |
NM_001126049.1:c.-577_-574del (KLLN) | NP_001119521.1:n.-577_-574del | |
NM_001126049.2:c.-577_-574del (KLLN) MANE Select | NP_001119521.1:n.-577_-574del |