Canonical Allele Identifier: CA891837155
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965320_87965322delinsTTT , CM000672.2:g.87965320_87965322delinsTTT GRCh38
NC_000010.10:g.89725077_89725079delinsTTT , CM000672.1:g.89725077_89725079delinsTTT GRCh37
NC_000010.9:g.89715057_89715059delinsTTT NCBI36
NG_007466.2:g.106882_106884delinsTTT , LRG_311:g.106882_106884delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1153_1155delinsTTT ENSP00000514759.2:p.Pro385Phe
ENST00000710265.1:c.*89_*91delinsTTT ENSP00000518161.1:n.*89_*91delinsTTT
ENST00000688158.2:n.1795_1797delinsTTT
ENST00000688922.2:c.*890_*892delinsTTT ENSP00000508742.2:n.*890_*892delinsTTT
ENST00000700021.1:c.1015_1017delinsTTT ENSP00000514757.1:p.Pro339Phe
ENST00000700022.1:c.*399_*401delinsTTT ENSP00000514758.1:n.*399_*401delinsTTT
ENST00000700023.1:n.2218_2220delinsTTT
ENST00000700024.1:n.2452_2454delinsTTT
ENST00000706954.1:c.1060_1062delinsTTT ENSP00000516674.1:p.Pro354Phe
ENST00000706955.1:c.*1095_*1097delinsTTT ENSP00000516675.1:n.*1095_*1097delinsTTT
ENST00000686459.1:c.*646_*648delinsTTT ENSP00000508909.1:n.*646_*648delinsTTT
ENST00000688158.1:c.*1171_*1173delinsTTT ENSP00000509254.1:n.*1171_*1173delinsTTT
ENST00000688308.1:c.1060_1062delinsTTT ENSP00000508752.1:p.Pro354Phe
ENST00000688922.1:c.981_983delinsTTT
ENST00000693560.1:c.1579_1581delinsTTT ENSP00000509861.1:p.Pro527Phe
ENST00000371953.8:c.1060_1062delinsTTT MANE Select ENSP00000361021.3:p.Pro354Phe
ENST00000371953.7:c.1060_1062delinsTTT ENSP00000361021.3:p.Pro354Phe
NM_000314.5:c.1060_1062delinsTTT NP_000305.3:p.Pro354Phe
NM_000314.6:c.1060_1062delinsTTT NP_000305.3:p.Pro354Phe
NM_001304717.2:c.1579_1581delinsTTT NP_001291646.2:p.Pro527Phe
NM_001304718.1:c.469_471delinsTTT NP_001291647.1:p.Pro157Phe
XM_006717926.2:c.1015_1017delinsTTT XP_006717989.1:p.Pro339Phe
XM_011539982.1:c.964_966delinsTTT XP_011538284.1:p.Pro322Phe
XR_945791.1:n.1630_1632delinsTTT
NM_000314.7:c.1060_1062delinsTTT NP_000305.3:p.Pro354Phe
NM_001304717.5:c.1579_1581delinsTTT NP_001291646.4:p.Pro527Phe
NM_001304718.2:c.469_471delinsTTT NP_001291647.1:p.Pro157Phe
NM_000314.8:c.1060_1062delinsTTT MANE Select NP_000305.3:p.Pro354Phe