Canonical Allele Identifier: CA891837320
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965338_87965340delinsCAA , CM000672.2:g.87965338_87965340delinsCAA GRCh38
NC_000010.10:g.89725095_89725097delinsCAA , CM000672.1:g.89725095_89725097delinsCAA GRCh37
NC_000010.9:g.89715075_89715077delinsCAA NCBI36
NG_007466.2:g.106900_106902delinsCAA , LRG_311:g.106900_106902delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1171_1173delinsCAA ENSP00000514759.2:p.Ser391Gln
ENST00000710265.1:c.*107_*109delinsCAA ENSP00000518161.1:n.*107_*109delinsCAA
ENST00000688158.2:n.1813_1815delinsCAA
ENST00000688922.2:c.*908_*910delinsCAA ENSP00000508742.2:n.*908_*910delinsCAA
ENST00000700021.1:c.1033_1035delinsCAA ENSP00000514757.1:p.Ser345Gln
ENST00000700022.1:c.*417_*419delinsCAA ENSP00000514758.1:n.*417_*419delinsCAA
ENST00000700023.1:n.2236_2238delinsCAA
ENST00000700024.1:n.2470_2472delinsCAA
ENST00000706954.1:c.1078_1080delinsCAA ENSP00000516674.1:p.Ser360Gln
ENST00000706955.1:c.*1113_*1115delinsCAA ENSP00000516675.1:n.*1113_*1115delinsCAA
ENST00000686459.1:c.*664_*666delinsCAA ENSP00000508909.1:n.*664_*666delinsCAA
ENST00000688158.1:c.*1189_*1191delinsCAA ENSP00000509254.1:n.*1189_*1191delinsCAA
ENST00000688308.1:c.1078_1080delinsCAA ENSP00000508752.1:p.Ser360Gln
ENST00000688922.1:c.999_1001delinsCAA
ENST00000693560.1:c.1597_1599delinsCAA ENSP00000509861.1:p.Ser533Gln
ENST00000371953.8:c.1078_1080delinsCAA MANE Select ENSP00000361021.3:p.Ser360Gln
ENST00000371953.7:c.1078_1080delinsCAA ENSP00000361021.3:p.Ser360Gln
NM_000314.5:c.1078_1080delinsCAA NP_000305.3:p.Ser360Gln
NM_000314.6:c.1078_1080delinsCAA NP_000305.3:p.Ser360Gln
NM_001304717.2:c.1597_1599delinsCAA NP_001291646.2:p.Ser533Gln
NM_001304718.1:c.487_489delinsCAA NP_001291647.1:p.Ser163Gln
XM_006717926.2:c.1033_1035delinsCAA XP_006717989.1:p.Ser345Gln
XM_011539982.1:c.982_984delinsCAA XP_011538284.1:p.Ser328Gln
XR_945791.1:n.1648_1650delinsCAA
NM_000314.7:c.1078_1080delinsCAA NP_000305.3:p.Ser360Gln
NM_001304717.5:c.1597_1599delinsCAA NP_001291646.4:p.Ser533Gln
NM_001304718.2:c.487_489delinsCAA NP_001291647.1:p.Ser163Gln
NM_000314.8:c.1078_1080delinsCAA MANE Select NP_000305.3:p.Ser360Gln