Canonical Allele Identifier: CA891837524
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965362_87965364delinsTAA , CM000672.2:g.87965362_87965364delinsTAA GRCh38
NC_000010.10:g.89725119_89725121delinsTAA , CM000672.1:g.89725119_89725121delinsTAA GRCh37
NC_000010.9:g.89715099_89715101delinsTAA NCBI36
NG_007466.2:g.106924_106926delinsTAA , LRG_311:g.106924_106926delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1195_1197delinsTAA ENSP00000514759.2:p.Asp399Ter
ENST00000710265.1:c.*131_*133delinsTAA ENSP00000518161.1:n.*131_*133delinsTAA
ENST00000688158.2:n.1837_1839delinsTAA
ENST00000688922.2:c.*932_*934delinsTAA ENSP00000508742.2:n.*932_*934delinsTAA
ENST00000700021.1:c.1057_1059delinsTAA ENSP00000514757.1:p.Asp353Ter
ENST00000700022.1:c.*441_*443delinsTAA ENSP00000514758.1:n.*441_*443delinsTAA
ENST00000700023.1:n.2260_2262delinsTAA
ENST00000700024.1:n.2494_2496delinsTAA
ENST00000706954.1:c.1102_1104delinsTAA ENSP00000516674.1:p.Asp368Ter
ENST00000706955.1:c.*1137_*1139delinsTAA ENSP00000516675.1:n.*1137_*1139delinsTAA
ENST00000686459.1:c.*688_*690delinsTAA ENSP00000508909.1:n.*688_*690delinsTAA
ENST00000688158.1:c.*1213_*1215delinsTAA ENSP00000509254.1:n.*1213_*1215delinsTAA
ENST00000688308.1:c.1102_1104delinsTAA ENSP00000508752.1:p.Asp368Ter
ENST00000688922.1:c.1023_1025delinsTAA
ENST00000693560.1:c.1621_1623delinsTAA ENSP00000509861.1:p.Asp541Ter
ENST00000371953.8:c.1102_1104delinsTAA MANE Select ENSP00000361021.3:p.Asp368Ter
ENST00000371953.7:c.1102_1104delinsTAA ENSP00000361021.3:p.Asp368Ter
NM_000314.5:c.1102_1104delinsTAA NP_000305.3:p.Asp368Ter
NM_000314.6:c.1102_1104delinsTAA NP_000305.3:p.Asp368Ter
NM_001304717.2:c.1621_1623delinsTAA NP_001291646.2:p.Asp541Ter
NM_001304718.1:c.511_513delinsTAA NP_001291647.1:p.Asp171Ter
XM_006717926.2:c.1057_1059delinsTAA XP_006717989.1:p.Asp353Ter
XM_011539982.1:c.1006_1008delinsTAA XP_011538284.1:p.Asp336Ter
XR_945791.1:n.1672_1674delinsTAA
NM_000314.7:c.1102_1104delinsTAA NP_000305.3:p.Asp368Ter
NM_001304717.5:c.1621_1623delinsTAA NP_001291646.4:p.Asp541Ter
NM_001304718.2:c.511_513delinsTAA NP_001291647.1:p.Asp171Ter
NM_000314.8:c.1102_1104delinsTAA MANE Select NP_000305.3:p.Asp368Ter