Canonical Allele Identifier: CA891837318
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965338_87965340delinsGGT , CM000672.2:g.87965338_87965340delinsGGT GRCh38
NC_000010.10:g.89725095_89725097delinsGGT , CM000672.1:g.89725095_89725097delinsGGT GRCh37
NC_000010.9:g.89715075_89715077delinsGGT NCBI36
NG_007466.2:g.106900_106902delinsGGT , LRG_311:g.106900_106902delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1171_1173delinsGGT ENSP00000514759.2:p.Ser391Gly
ENST00000710265.1:c.*107_*109delinsGGT ENSP00000518161.1:n.*107_*109delinsGGT
ENST00000688158.2:n.1813_1815delinsGGT
ENST00000688922.2:c.*908_*910delinsGGT ENSP00000508742.2:n.*908_*910delinsGGT
ENST00000700021.1:c.1033_1035delinsGGT ENSP00000514757.1:p.Ser345Gly
ENST00000700022.1:c.*417_*419delinsGGT ENSP00000514758.1:n.*417_*419delinsGGT
ENST00000700023.1:n.2236_2238delinsGGT
ENST00000700024.1:n.2470_2472delinsGGT
ENST00000706954.1:c.1078_1080delinsGGT ENSP00000516674.1:p.Ser360Gly
ENST00000706955.1:c.*1113_*1115delinsGGT ENSP00000516675.1:n.*1113_*1115delinsGGT
ENST00000686459.1:c.*664_*666delinsGGT ENSP00000508909.1:n.*664_*666delinsGGT
ENST00000688158.1:c.*1189_*1191delinsGGT ENSP00000509254.1:n.*1189_*1191delinsGGT
ENST00000688308.1:c.1078_1080delinsGGT ENSP00000508752.1:p.Ser360Gly
ENST00000688922.1:c.999_1001delinsGGT
ENST00000693560.1:c.1597_1599delinsGGT ENSP00000509861.1:p.Ser533Gly
ENST00000371953.8:c.1078_1080delinsGGT MANE Select ENSP00000361021.3:p.Ser360Gly
ENST00000371953.7:c.1078_1080delinsGGT ENSP00000361021.3:p.Ser360Gly
NM_000314.5:c.1078_1080delinsGGT NP_000305.3:p.Ser360Gly
NM_000314.6:c.1078_1080delinsGGT NP_000305.3:p.Ser360Gly
NM_001304717.2:c.1597_1599delinsGGT NP_001291646.2:p.Ser533Gly
NM_001304718.1:c.487_489delinsGGT NP_001291647.1:p.Ser163Gly
XM_006717926.2:c.1033_1035delinsGGT XP_006717989.1:p.Ser345Gly
XM_011539982.1:c.982_984delinsGGT XP_011538284.1:p.Ser328Gly
XR_945791.1:n.1648_1650delinsGGT
NM_000314.7:c.1078_1080delinsGGT NP_000305.3:p.Ser360Gly
NM_001304717.5:c.1597_1599delinsGGT NP_001291646.4:p.Ser533Gly
NM_001304718.2:c.487_489delinsGGT NP_001291647.1:p.Ser163Gly
NM_000314.8:c.1078_1080delinsGGT MANE Select NP_000305.3:p.Ser360Gly