HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863056_87863059del , CM000672.2:g.87863056_87863059del | GRCh38 |
NC_000010.10:g.89622813_89622816del , CM000672.1:g.89622813_89622816del | GRCh37 |
NC_000010.9:g.89612793_89612796del | NCBI36 |
NG_007466.2:g.4619_4622del , LRG_311:g.4619_4622del | |
NG_033079.1:g.5380_5383del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+414_-17+417del (PTEN) | ENSP00000516674.1:n.-17+414_-17+417del | |
ENST00000688308.1:c.-74_-71del (PTEN) | ENSP00000508752.1:n.-74_-71del | |
ENST00000445946.5:c.-571_-568del (KLLN) MANE Select | ENSP00000392204.2:n.-571_-568del | |
ENST00000445946.3:c.-571_-568del (KLLN) | ENSP00000392204.2:n.-571_-568del | |
NM_001126049.1:c.-571_-568del (KLLN) | NP_001119521.1:n.-571_-568del | |
NM_001126049.2:c.-571_-568del (KLLN) MANE Select | NP_001119521.1:n.-571_-568del |