Canonical Allele Identifier: CA891837589
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965369_87965370delinsTG , CM000672.2:g.87965369_87965370delinsTG GRCh38
NC_000010.10:g.89725126_89725127delinsTG , CM000672.1:g.89725126_89725127delinsTG GRCh37
NC_000010.9:g.89715106_89715107delinsTG NCBI36
NG_007466.2:g.106931_106932delinsTG , LRG_311:g.106931_106932delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1202_1203delinsTG ENSP00000514759.2:p.Ser401Met
ENST00000710265.1:c.*138_*139delinsTG ENSP00000518161.1:n.*138_*139delinsTG
ENST00000688158.2:n.1844_1845delinsTG
ENST00000688922.2:c.*939_*940delinsTG ENSP00000508742.2:n.*939_*940delinsTG
ENST00000700021.1:c.1064_1065delinsTG ENSP00000514757.1:p.Ser355Met
ENST00000700022.1:c.*448_*449delinsTG ENSP00000514758.1:n.*448_*449delinsTG
ENST00000700023.1:n.2267_2268delinsTG
ENST00000700024.1:n.2501_2502delinsTG
ENST00000706954.1:c.1109_1110delinsTG ENSP00000516674.1:p.Ser370Met
ENST00000706955.1:c.*1144_*1145delinsTG ENSP00000516675.1:n.*1144_*1145delinsTG
ENST00000686459.1:c.*695_*696delinsTG ENSP00000508909.1:n.*695_*696delinsTG
ENST00000688158.1:c.*1220_*1221delinsTG ENSP00000509254.1:n.*1220_*1221delinsTG
ENST00000688308.1:c.1109_1110delinsTG ENSP00000508752.1:p.Ser370Met
ENST00000688922.1:c.1030_1031delinsTG
ENST00000693560.1:c.1628_1629delinsTG ENSP00000509861.1:p.Ser543Met
ENST00000371953.8:c.1109_1110delinsTG MANE Select ENSP00000361021.3:p.Ser370Met
ENST00000371953.7:c.1109_1110delinsTG ENSP00000361021.3:p.Ser370Met
NM_000314.5:c.1109_1110delinsTG NP_000305.3:p.Ser370Met
NM_000314.6:c.1109_1110delinsTG NP_000305.3:p.Ser370Met
NM_001304717.2:c.1628_1629delinsTG NP_001291646.2:p.Ser543Met
NM_001304718.1:c.518_519delinsTG NP_001291647.1:p.Ser173Met
XM_006717926.2:c.1064_1065delinsTG XP_006717989.1:p.Ser355Met
XM_011539982.1:c.1013_1014delinsTG XP_011538284.1:p.Ser338Met
XR_945791.1:n.1679_1680delinsTG
NM_000314.7:c.1109_1110delinsTG NP_000305.3:p.Ser370Met
NM_001304717.5:c.1628_1629delinsTG NP_001291646.4:p.Ser543Met
NM_001304718.2:c.518_519delinsTG NP_001291647.1:p.Ser173Met
NM_000314.8:c.1109_1110delinsTG MANE Select NP_000305.3:p.Ser370Met