Canonical Allele Identifier: CA891837533
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965362_87965364delinsATG , CM000672.2:g.87965362_87965364delinsATG GRCh38
NC_000010.10:g.89725119_89725121delinsATG , CM000672.1:g.89725119_89725121delinsATG GRCh37
NC_000010.9:g.89715099_89715101delinsATG NCBI36
NG_007466.2:g.106924_106926delinsATG , LRG_311:g.106924_106926delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1195_1197delinsATG ENSP00000514759.2:p.Asp399Met
ENST00000710265.1:c.*131_*133delinsATG ENSP00000518161.1:n.*131_*133delinsATG
ENST00000688158.2:n.1837_1839delinsATG
ENST00000688922.2:c.*932_*934delinsATG ENSP00000508742.2:n.*932_*934delinsATG
ENST00000700021.1:c.1057_1059delinsATG ENSP00000514757.1:p.Asp353Met
ENST00000700022.1:c.*441_*443delinsATG ENSP00000514758.1:n.*441_*443delinsATG
ENST00000700023.1:n.2260_2262delinsATG
ENST00000700024.1:n.2494_2496delinsATG
ENST00000706954.1:c.1102_1104delinsATG ENSP00000516674.1:p.Asp368Met
ENST00000706955.1:c.*1137_*1139delinsATG ENSP00000516675.1:n.*1137_*1139delinsATG
ENST00000686459.1:c.*688_*690delinsATG ENSP00000508909.1:n.*688_*690delinsATG
ENST00000688158.1:c.*1213_*1215delinsATG ENSP00000509254.1:n.*1213_*1215delinsATG
ENST00000688308.1:c.1102_1104delinsATG ENSP00000508752.1:p.Asp368Met
ENST00000688922.1:c.1023_1025delinsATG
ENST00000693560.1:c.1621_1623delinsATG ENSP00000509861.1:p.Asp541Met
ENST00000371953.8:c.1102_1104delinsATG MANE Select ENSP00000361021.3:p.Asp368Met
ENST00000371953.7:c.1102_1104delinsATG ENSP00000361021.3:p.Asp368Met
NM_000314.5:c.1102_1104delinsATG NP_000305.3:p.Asp368Met
NM_000314.6:c.1102_1104delinsATG NP_000305.3:p.Asp368Met
NM_001304717.2:c.1621_1623delinsATG NP_001291646.2:p.Asp541Met
NM_001304718.1:c.511_513delinsATG NP_001291647.1:p.Asp171Met
XM_006717926.2:c.1057_1059delinsATG XP_006717989.1:p.Asp353Met
XM_011539982.1:c.1006_1008delinsATG XP_011538284.1:p.Asp336Met
XR_945791.1:n.1672_1674delinsATG
NM_000314.7:c.1102_1104delinsATG NP_000305.3:p.Asp368Met
NM_001304717.5:c.1621_1623delinsATG NP_001291646.4:p.Asp541Met
NM_001304718.2:c.511_513delinsATG NP_001291647.1:p.Asp171Met
NM_000314.8:c.1102_1104delinsATG MANE Select NP_000305.3:p.Asp368Met