Canonical Allele Identifier: CA891837875
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965401_87965403delinsCCA , CM000672.2:g.87965401_87965403delinsCCA GRCh38
NC_000010.10:g.89725158_89725160delinsCCA , CM000672.1:g.89725158_89725160delinsCCA GRCh37
NC_000010.9:g.89715138_89715140delinsCCA NCBI36
NG_007466.2:g.106963_106965delinsCCA , LRG_311:g.106963_106965delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1234_1236delinsCCA ENSP00000514759.2:p.Asp412Pro
ENST00000710265.1:c.*170_*172delinsCCA ENSP00000518161.1:n.*170_*172delinsCCA
ENST00000688158.2:n.1876_1878delinsCCA
ENST00000688922.2:c.*971_*973delinsCCA ENSP00000508742.2:n.*971_*973delinsCCA
ENST00000700021.1:c.1096_1098delinsCCA ENSP00000514757.1:p.Asp366Pro
ENST00000700022.1:c.*480_*482delinsCCA ENSP00000514758.1:n.*480_*482delinsCCA
ENST00000700023.1:n.2299_2301delinsCCA
ENST00000700024.1:n.2533_2535delinsCCA
ENST00000706954.1:c.1141_1143delinsCCA ENSP00000516674.1:p.Asp381Pro
ENST00000706955.1:c.*1176_*1178delinsCCA ENSP00000516675.1:n.*1176_*1178delinsCCA
ENST00000686459.1:c.*727_*729delinsCCA ENSP00000508909.1:n.*727_*729delinsCCA
ENST00000688158.1:c.*1252_*1254delinsCCA ENSP00000509254.1:n.*1252_*1254delinsCCA
ENST00000688308.1:c.1141_1143delinsCCA ENSP00000508752.1:p.Asp381Pro
ENST00000688922.1:c.1062_1064delinsCCA
ENST00000693560.1:c.1660_1662delinsCCA ENSP00000509861.1:p.Asp554Pro
ENST00000371953.8:c.1141_1143delinsCCA MANE Select ENSP00000361021.3:p.Asp381Pro
ENST00000371953.7:c.1141_1143delinsCCA ENSP00000361021.3:p.Asp381Pro
NM_000314.5:c.1141_1143delinsCCA NP_000305.3:p.Asp381Pro
NM_000314.6:c.1141_1143delinsCCA NP_000305.3:p.Asp381Pro
NM_001304717.2:c.1660_1662delinsCCA NP_001291646.2:p.Asp554Pro
NM_001304718.1:c.550_552delinsCCA NP_001291647.1:p.Asp184Pro
XM_006717926.2:c.1096_1098delinsCCA XP_006717989.1:p.Asp366Pro
XM_011539982.1:c.1045_1047delinsCCA XP_011538284.1:p.Asp349Pro
XR_945791.1:n.1711_1713delinsCCA
NM_000314.7:c.1141_1143delinsCCA NP_000305.3:p.Asp381Pro
NM_001304717.5:c.1660_1662delinsCCA NP_001291646.4:p.Asp554Pro
NM_001304718.2:c.550_552delinsCCA NP_001291647.1:p.Asp184Pro
NM_000314.8:c.1141_1143delinsCCA MANE Select NP_000305.3:p.Asp381Pro