Canonical Allele Identifier: CA891838181
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965449_87965451delinsGAA , CM000672.2:g.87965449_87965451delinsGAA GRCh38
NC_000010.10:g.89725206_89725208delinsGAA , CM000672.1:g.89725206_89725208delinsGAA GRCh37
NC_000010.9:g.89715186_89715188delinsGAA NCBI36
NG_007466.2:g.107011_107013delinsGAA , LRG_311:g.107011_107013delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1282_1284delinsGAA ENSP00000514759.2:p.His428Glu
ENST00000710265.1:c.*218_*220delinsGAA ENSP00000518161.1:n.*218_*220delinsGAA
ENST00000688158.2:n.1924_1926delinsGAA
ENST00000688922.2:c.*1019_*1021delinsGAA ENSP00000508742.2:n.*1019_*1021delinsGAA
ENST00000700021.1:c.1144_1146delinsGAA ENSP00000514757.1:p.His382Glu
ENST00000700022.1:c.*528_*530delinsGAA ENSP00000514758.1:n.*528_*530delinsGAA
ENST00000700023.1:n.2347_2349delinsGAA
ENST00000700024.1:n.2581_2583delinsGAA
ENST00000706954.1:c.1189_1191delinsGAA ENSP00000516674.1:p.His397Glu
ENST00000706955.1:c.*1224_*1226delinsGAA ENSP00000516675.1:n.*1224_*1226delinsGAA
ENST00000686459.1:c.*775_*777delinsGAA ENSP00000508909.1:n.*775_*777delinsGAA
ENST00000688158.1:c.*1300_*1302delinsGAA ENSP00000509254.1:n.*1300_*1302delinsGAA
ENST00000688308.1:c.1189_1191delinsGAA ENSP00000508752.1:p.His397Glu
ENST00000688922.1:c.1110_1112delinsGAA
ENST00000693560.1:c.1708_1710delinsGAA ENSP00000509861.1:p.His570Glu
ENST00000371953.8:c.1189_1191delinsGAA MANE Select ENSP00000361021.3:p.His397Glu
ENST00000371953.7:c.1189_1191delinsGAA ENSP00000361021.3:p.His397Glu
NM_000314.5:c.1189_1191delinsGAA NP_000305.3:p.His397Glu
NM_000314.6:c.1189_1191delinsGAA NP_000305.3:p.His397Glu
NM_001304717.2:c.1708_1710delinsGAA NP_001291646.2:p.His570Glu
NM_001304718.1:c.598_600delinsGAA NP_001291647.1:p.His200Glu
XM_006717926.2:c.1144_1146delinsGAA XP_006717989.1:p.His382Glu
XM_011539982.1:c.1093_1095delinsGAA XP_011538284.1:p.His365Glu
XR_945791.1:n.1759_1761delinsGAA
NM_000314.7:c.1189_1191delinsGAA NP_000305.3:p.His397Glu
NM_001304717.5:c.1708_1710delinsGAA NP_001291646.4:p.His570Glu
NM_001304718.2:c.598_600delinsGAA NP_001291647.1:p.His200Glu
NM_000314.8:c.1189_1191delinsGAA MANE Select NP_000305.3:p.His397Glu