Canonical Allele Identifier: CA891837872
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965401_87965403delinsTAA , CM000672.2:g.87965401_87965403delinsTAA GRCh38
NC_000010.10:g.89725158_89725160delinsTAA , CM000672.1:g.89725158_89725160delinsTAA GRCh37
NC_000010.9:g.89715138_89715140delinsTAA NCBI36
NG_007466.2:g.106963_106965delinsTAA , LRG_311:g.106963_106965delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1234_1236delinsTAA ENSP00000514759.2:p.Asp412Ter
ENST00000710265.1:c.*170_*172delinsTAA ENSP00000518161.1:n.*170_*172delinsTAA
ENST00000688158.2:n.1876_1878delinsTAA
ENST00000688922.2:c.*971_*973delinsTAA ENSP00000508742.2:n.*971_*973delinsTAA
ENST00000700021.1:c.1096_1098delinsTAA ENSP00000514757.1:p.Asp366Ter
ENST00000700022.1:c.*480_*482delinsTAA ENSP00000514758.1:n.*480_*482delinsTAA
ENST00000700023.1:n.2299_2301delinsTAA
ENST00000700024.1:n.2533_2535delinsTAA
ENST00000706954.1:c.1141_1143delinsTAA ENSP00000516674.1:p.Asp381Ter
ENST00000706955.1:c.*1176_*1178delinsTAA ENSP00000516675.1:n.*1176_*1178delinsTAA
ENST00000686459.1:c.*727_*729delinsTAA ENSP00000508909.1:n.*727_*729delinsTAA
ENST00000688158.1:c.*1252_*1254delinsTAA ENSP00000509254.1:n.*1252_*1254delinsTAA
ENST00000688308.1:c.1141_1143delinsTAA ENSP00000508752.1:p.Asp381Ter
ENST00000688922.1:c.1062_1064delinsTAA
ENST00000693560.1:c.1660_1662delinsTAA ENSP00000509861.1:p.Asp554Ter
ENST00000371953.8:c.1141_1143delinsTAA MANE Select ENSP00000361021.3:p.Asp381Ter
ENST00000371953.7:c.1141_1143delinsTAA ENSP00000361021.3:p.Asp381Ter
NM_000314.5:c.1141_1143delinsTAA NP_000305.3:p.Asp381Ter
NM_000314.6:c.1141_1143delinsTAA NP_000305.3:p.Asp381Ter
NM_001304717.2:c.1660_1662delinsTAA NP_001291646.2:p.Asp554Ter
NM_001304718.1:c.550_552delinsTAA NP_001291647.1:p.Asp184Ter
XM_006717926.2:c.1096_1098delinsTAA XP_006717989.1:p.Asp366Ter
XM_011539982.1:c.1045_1047delinsTAA XP_011538284.1:p.Asp349Ter
XR_945791.1:n.1711_1713delinsTAA
NM_000314.7:c.1141_1143delinsTAA NP_000305.3:p.Asp381Ter
NM_001304717.5:c.1660_1662delinsTAA NP_001291646.4:p.Asp554Ter
NM_001304718.2:c.550_552delinsTAA NP_001291647.1:p.Asp184Ter
NM_000314.8:c.1141_1143delinsTAA MANE Select NP_000305.3:p.Asp381Ter