Canonical Allele Identifier: CA891837327
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965338_87965340delinsTAA , CM000672.2:g.87965338_87965340delinsTAA GRCh38
NC_000010.10:g.89725095_89725097delinsTAA , CM000672.1:g.89725095_89725097delinsTAA GRCh37
NC_000010.9:g.89715075_89715077delinsTAA NCBI36
NG_007466.2:g.106900_106902delinsTAA , LRG_311:g.106900_106902delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1171_1173delinsTAA ENSP00000514759.2:p.Ser391Ter
ENST00000710265.1:c.*107_*109delinsTAA ENSP00000518161.1:n.*107_*109delinsTAA
ENST00000688158.2:n.1813_1815delinsTAA
ENST00000688922.2:c.*908_*910delinsTAA ENSP00000508742.2:n.*908_*910delinsTAA
ENST00000700021.1:c.1033_1035delinsTAA ENSP00000514757.1:p.Ser345Ter
ENST00000700022.1:c.*417_*419delinsTAA ENSP00000514758.1:n.*417_*419delinsTAA
ENST00000700023.1:n.2236_2238delinsTAA
ENST00000700024.1:n.2470_2472delinsTAA
ENST00000706954.1:c.1078_1080delinsTAA ENSP00000516674.1:p.Ser360Ter
ENST00000706955.1:c.*1113_*1115delinsTAA ENSP00000516675.1:n.*1113_*1115delinsTAA
ENST00000686459.1:c.*664_*666delinsTAA ENSP00000508909.1:n.*664_*666delinsTAA
ENST00000688158.1:c.*1189_*1191delinsTAA ENSP00000509254.1:n.*1189_*1191delinsTAA
ENST00000688308.1:c.1078_1080delinsTAA ENSP00000508752.1:p.Ser360Ter
ENST00000688922.1:c.999_1001delinsTAA
ENST00000693560.1:c.1597_1599delinsTAA ENSP00000509861.1:p.Ser533Ter
ENST00000371953.8:c.1078_1080delinsTAA MANE Select ENSP00000361021.3:p.Ser360Ter
ENST00000371953.7:c.1078_1080delinsTAA ENSP00000361021.3:p.Ser360Ter
NM_000314.5:c.1078_1080delinsTAA NP_000305.3:p.Ser360Ter
NM_000314.6:c.1078_1080delinsTAA NP_000305.3:p.Ser360Ter
NM_001304717.2:c.1597_1599delinsTAA NP_001291646.2:p.Ser533Ter
NM_001304718.1:c.487_489delinsTAA NP_001291647.1:p.Ser163Ter
XM_006717926.2:c.1033_1035delinsTAA XP_006717989.1:p.Ser345Ter
XM_011539982.1:c.982_984delinsTAA XP_011538284.1:p.Ser328Ter
XR_945791.1:n.1648_1650delinsTAA
NM_000314.7:c.1078_1080delinsTAA NP_000305.3:p.Ser360Ter
NM_001304717.5:c.1597_1599delinsTAA NP_001291646.4:p.Ser533Ter
NM_001304718.2:c.487_489delinsTAA NP_001291647.1:p.Ser163Ter
NM_000314.8:c.1078_1080delinsTAA MANE Select NP_000305.3:p.Ser360Ter