Canonical Allele Identifier: CA891837395
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965345_87965346delinsTT , CM000672.2:g.87965345_87965346delinsTT GRCh38
NC_000010.10:g.89725102_89725103delinsTT , CM000672.1:g.89725102_89725103delinsTT GRCh37
NC_000010.9:g.89715082_89715083delinsTT NCBI36
NG_007466.2:g.106907_106908delinsTT , LRG_311:g.106907_106908delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1178_1179delinsTT ENSP00000514759.2:p.Ser393Phe
ENST00000710265.1:c.*114_*115delinsTT ENSP00000518161.1:n.*114_*115delinsTT
ENST00000688158.2:n.1820_1821delinsTT
ENST00000688922.2:c.*915_*916delinsTT ENSP00000508742.2:n.*915_*916delinsTT
ENST00000700021.1:c.1040_1041delinsTT ENSP00000514757.1:p.Ser347Phe
ENST00000700022.1:c.*424_*425delinsTT ENSP00000514758.1:n.*424_*425delinsTT
ENST00000700023.1:n.2243_2244delinsTT
ENST00000700024.1:n.2477_2478delinsTT
ENST00000706954.1:c.1085_1086delinsTT ENSP00000516674.1:p.Ser362Phe
ENST00000706955.1:c.*1120_*1121delinsTT ENSP00000516675.1:n.*1120_*1121delinsTT
ENST00000686459.1:c.*671_*672delinsTT ENSP00000508909.1:n.*671_*672delinsTT
ENST00000688158.1:c.*1196_*1197delinsTT ENSP00000509254.1:n.*1196_*1197delinsTT
ENST00000688308.1:c.1085_1086delinsTT ENSP00000508752.1:p.Ser362Phe
ENST00000688922.1:c.1006_1007delinsTT
ENST00000693560.1:c.1604_1605delinsTT ENSP00000509861.1:p.Ser535Phe
ENST00000371953.8:c.1085_1086delinsTT MANE Select ENSP00000361021.3:p.Ser362Phe
ENST00000371953.7:c.1085_1086delinsTT ENSP00000361021.3:p.Ser362Phe
NM_000314.5:c.1085_1086delinsTT NP_000305.3:p.Ser362Phe
NM_000314.6:c.1085_1086delinsTT NP_000305.3:p.Ser362Phe
NM_001304717.2:c.1604_1605delinsTT NP_001291646.2:p.Ser535Phe
NM_001304718.1:c.494_495delinsTT NP_001291647.1:p.Ser165Phe
XM_006717926.2:c.1040_1041delinsTT XP_006717989.1:p.Ser347Phe
XM_011539982.1:c.989_990delinsTT XP_011538284.1:p.Ser330Phe
XR_945791.1:n.1655_1656delinsTT
NM_000314.7:c.1085_1086delinsTT NP_000305.3:p.Ser362Phe
NM_001304717.5:c.1604_1605delinsTT NP_001291646.4:p.Ser535Phe
NM_001304718.2:c.494_495delinsTT NP_001291647.1:p.Ser165Phe
NM_000314.8:c.1085_1086delinsTT MANE Select NP_000305.3:p.Ser362Phe