Canonical Allele Identifier: CA891837319
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965338_87965340delinsTGT , CM000672.2:g.87965338_87965340delinsTGT GRCh38
NC_000010.10:g.89725095_89725097delinsTGT , CM000672.1:g.89725095_89725097delinsTGT GRCh37
NC_000010.9:g.89715075_89715077delinsTGT NCBI36
NG_007466.2:g.106900_106902delinsTGT , LRG_311:g.106900_106902delinsTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1171_1173delinsTGT ENSP00000514759.2:p.Ser391Cys
ENST00000710265.1:c.*107_*109delinsTGT ENSP00000518161.1:n.*107_*109delinsTGT
ENST00000688158.2:n.1813_1815delinsTGT
ENST00000688922.2:c.*908_*910delinsTGT ENSP00000508742.2:n.*908_*910delinsTGT
ENST00000700021.1:c.1033_1035delinsTGT ENSP00000514757.1:p.Ser345Cys
ENST00000700022.1:c.*417_*419delinsTGT ENSP00000514758.1:n.*417_*419delinsTGT
ENST00000700023.1:n.2236_2238delinsTGT
ENST00000700024.1:n.2470_2472delinsTGT
ENST00000706954.1:c.1078_1080delinsTGT ENSP00000516674.1:p.Ser360Cys
ENST00000706955.1:c.*1113_*1115delinsTGT ENSP00000516675.1:n.*1113_*1115delinsTGT
ENST00000686459.1:c.*664_*666delinsTGT ENSP00000508909.1:n.*664_*666delinsTGT
ENST00000688158.1:c.*1189_*1191delinsTGT ENSP00000509254.1:n.*1189_*1191delinsTGT
ENST00000688308.1:c.1078_1080delinsTGT ENSP00000508752.1:p.Ser360Cys
ENST00000688922.1:c.999_1001delinsTGT
ENST00000693560.1:c.1597_1599delinsTGT ENSP00000509861.1:p.Ser533Cys
ENST00000371953.8:c.1078_1080delinsTGT MANE Select ENSP00000361021.3:p.Ser360Cys
ENST00000371953.7:c.1078_1080delinsTGT ENSP00000361021.3:p.Ser360Cys
NM_000314.5:c.1078_1080delinsTGT NP_000305.3:p.Ser360Cys
NM_000314.6:c.1078_1080delinsTGT NP_000305.3:p.Ser360Cys
NM_001304717.2:c.1597_1599delinsTGT NP_001291646.2:p.Ser533Cys
NM_001304718.1:c.487_489delinsTGT NP_001291647.1:p.Ser163Cys
XM_006717926.2:c.1033_1035delinsTGT XP_006717989.1:p.Ser345Cys
XM_011539982.1:c.982_984delinsTGT XP_011538284.1:p.Ser328Cys
XR_945791.1:n.1648_1650delinsTGT
NM_000314.7:c.1078_1080delinsTGT NP_000305.3:p.Ser360Cys
NM_001304717.5:c.1597_1599delinsTGT NP_001291646.4:p.Ser533Cys
NM_001304718.2:c.487_489delinsTGT NP_001291647.1:p.Ser163Cys
NM_000314.8:c.1078_1080delinsTGT MANE Select NP_000305.3:p.Ser360Cys