Canonical Allele Identifier: CA891837152
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965320_87965322delinsGCT , CM000672.2:g.87965320_87965322delinsGCT GRCh38
NC_000010.10:g.89725077_89725079delinsGCT , CM000672.1:g.89725077_89725079delinsGCT GRCh37
NC_000010.9:g.89715057_89715059delinsGCT NCBI36
NG_007466.2:g.106882_106884delinsGCT , LRG_311:g.106882_106884delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1153_1155delinsGCT ENSP00000514759.2:p.Pro385Ala
ENST00000710265.1:c.*89_*91delinsGCT ENSP00000518161.1:n.*89_*91delinsGCT
ENST00000688158.2:n.1795_1797delinsGCT
ENST00000688922.2:c.*890_*892delinsGCT ENSP00000508742.2:n.*890_*892delinsGCT
ENST00000700021.1:c.1015_1017delinsGCT ENSP00000514757.1:p.Pro339Ala
ENST00000700022.1:c.*399_*401delinsGCT ENSP00000514758.1:n.*399_*401delinsGCT
ENST00000700023.1:n.2218_2220delinsGCT
ENST00000700024.1:n.2452_2454delinsGCT
ENST00000706954.1:c.1060_1062delinsGCT ENSP00000516674.1:p.Pro354Ala
ENST00000706955.1:c.*1095_*1097delinsGCT ENSP00000516675.1:n.*1095_*1097delinsGCT
ENST00000686459.1:c.*646_*648delinsGCT ENSP00000508909.1:n.*646_*648delinsGCT
ENST00000688158.1:c.*1171_*1173delinsGCT ENSP00000509254.1:n.*1171_*1173delinsGCT
ENST00000688308.1:c.1060_1062delinsGCT ENSP00000508752.1:p.Pro354Ala
ENST00000688922.1:c.981_983delinsGCT
ENST00000693560.1:c.1579_1581delinsGCT ENSP00000509861.1:p.Pro527Ala
ENST00000371953.8:c.1060_1062delinsGCT MANE Select ENSP00000361021.3:p.Pro354Ala
ENST00000371953.7:c.1060_1062delinsGCT ENSP00000361021.3:p.Pro354Ala
NM_000314.5:c.1060_1062delinsGCT NP_000305.3:p.Pro354Ala
NM_000314.6:c.1060_1062delinsGCT NP_000305.3:p.Pro354Ala
NM_001304717.2:c.1579_1581delinsGCT NP_001291646.2:p.Pro527Ala
NM_001304718.1:c.469_471delinsGCT NP_001291647.1:p.Pro157Ala
XM_006717926.2:c.1015_1017delinsGCT XP_006717989.1:p.Pro339Ala
XM_011539982.1:c.964_966delinsGCT XP_011538284.1:p.Pro322Ala
XR_945791.1:n.1630_1632delinsGCT
NM_000314.7:c.1060_1062delinsGCT NP_000305.3:p.Pro354Ala
NM_001304717.5:c.1579_1581delinsGCT NP_001291646.4:p.Pro527Ala
NM_001304718.2:c.469_471delinsGCT NP_001291647.1:p.Pro157Ala
NM_000314.8:c.1060_1062delinsGCT MANE Select NP_000305.3:p.Pro354Ala