Canonical Allele Identifier: CA3057286925
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933167del , CM000672.2:g.87933167del GRCh38
NC_000010.10:g.89692924del , CM000672.1:g.89692924del GRCh37
NC_000010.9:g.89682904del NCBI36
NG_007466.2:g.74729del , LRG_311:g.74729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.408del ENSP00000514759.2:p.Cys136TrpfsTer11
ENST00000710265.1:c.408del ENSP00000518161.1:p.Cys136TrpfsTer11
ENST00000472832.3:c.408del ENSP00000483066.2:p.Cys136TrpfsTer11
ENST00000688158.2:n.1143del
ENST00000688922.2:c.*238del ENSP00000508742.2:n.*238del
ENST00000700021.1:c.363del ENSP00000514757.1:p.Cys121TrpfsTer11
ENST00000700022.1:c.408del ENSP00000514758.1:p.Cys136TrpfsTer11
ENST00000700029.1:c.242del
ENST00000706954.1:c.408del ENSP00000516674.1:p.Cys136TrpfsTer11
ENST00000706955.1:c.*443del ENSP00000516675.1:n.*443del
ENST00000686459.1:c.408del ENSP00000508909.1:p.Cys136TrpfsTer11
ENST00000688158.1:c.*519del ENSP00000509254.1:n.*519del
ENST00000688308.1:c.408del ENSP00000508752.1:p.Cys136TrpfsTer11
ENST00000688922.1:c.329del
ENST00000693560.1:c.927del ENSP00000509861.1:p.Cys309TrpfsTer11
ENST00000371953.8:c.408del MANE Select ENSP00000361021.3:p.Cys136TrpfsTer11
ENST00000371953.7:c.408del ENSP00000361021.3:p.Cys136TrpfsTer11
ENST00000498703.1:n.234del
ENST00000610634.1:c.306del ENSP00000477517.1:p.Cys102TrpfsTer11
NM_000314.5:c.408del NP_000305.3:p.Cys136TrpfsTer11
NM_000314.6:c.408del NP_000305.3:p.Cys136TrpfsTer11
NM_001304717.2:c.927del NP_001291646.2:p.Cys309TrpfsTer11
NM_001304718.1:c.-343del NP_001291647.1:n.-343del
XM_006717926.2:c.363del XP_006717989.1:p.Cys121TrpfsTer11
XM_011539981.1:c.408del XP_011538283.1:p.Cys136TrpfsTer11
XM_011539982.1:c.312del XP_011538284.1:p.Cys104TrpfsTer11
XR_945789.1:n.1120del
XR_945790.1:n.1120del
XR_945791.1:n.1120del
NM_000314.7:c.408del NP_000305.3:p.Cys136TrpfsTer11
NM_001304717.5:c.927del NP_001291646.4:p.Cys309TrpfsTer11
NM_001304718.2:c.-343del NP_001291647.1:n.-343del
NM_000314.8:c.408del MANE Select NP_000305.3:p.Cys136TrpfsTer11