Canonical Allele Identifier: CA891837626
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965376delinsGAA , CM000672.2:g.87965374_87965376delinsGAA GRCh38
NC_000010.10:g.89725131_89725133delinsGAA , CM000672.1:g.89725131_89725133delinsGAA GRCh37
NC_000010.9:g.89715111_89715113delinsGAA NCBI36
NG_007466.2:g.106936_106938delinsGAA , LRG_311:g.106936_106938delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1209delinsGAA ENSP00000514759.2:p.Asn403Glu
ENST00000710265.1:c.*143_*145delinsGAA ENSP00000518161.1:n.*143_*145delinsGAA
ENST00000688158.2:n.1849_1851delinsGAA
ENST00000688922.2:c.*944_*946delinsGAA ENSP00000508742.2:n.*944_*946delinsGAA
ENST00000700021.1:c.1069_1071delinsGAA ENSP00000514757.1:p.Asn357Glu
ENST00000700022.1:c.*453_*455delinsGAA ENSP00000514758.1:n.*453_*455delinsGAA
ENST00000700023.1:n.2272_2274delinsGAA
ENST00000700024.1:n.2506_2508delinsGAA
ENST00000706954.1:c.1114_1116delinsGAA ENSP00000516674.1:p.Asn372Glu
ENST00000706955.1:c.*1149_*1151delinsGAA ENSP00000516675.1:n.*1149_*1151delinsGAA
ENST00000686459.1:c.*700_*702delinsGAA ENSP00000508909.1:n.*700_*702delinsGAA
ENST00000688158.1:c.*1225_*1227delinsGAA ENSP00000509254.1:n.*1225_*1227delinsGAA
ENST00000688308.1:c.1114_1116delinsGAA ENSP00000508752.1:p.Asn372Glu
ENST00000688922.1:c.1035_1037delinsGAA
ENST00000693560.1:c.1633_1635delinsGAA ENSP00000509861.1:p.Asn545Glu
ENST00000371953.8:c.1114_1116delinsGAA MANE Select ENSP00000361021.3:p.Asn372Glu
ENST00000371953.7:c.1114_1116delinsGAA ENSP00000361021.3:p.Asn372Glu
NM_000314.5:c.1114_1116delinsGAA NP_000305.3:p.Asn372Glu
NM_000314.6:c.1114_1116delinsGAA NP_000305.3:p.Asn372Glu
NM_001304717.2:c.1633_1635delinsGAA NP_001291646.2:p.Asn545Glu
NM_001304718.1:c.523_525delinsGAA NP_001291647.1:p.Asn175Glu
XM_006717926.2:c.1069_1071delinsGAA XP_006717989.1:p.Asn357Glu
XM_011539982.1:c.1018_1020delinsGAA XP_011538284.1:p.Asn340Glu
XR_945791.1:n.1684_1686delinsGAA
NM_000314.7:c.1114_1116delinsGAA NP_000305.3:p.Asn372Glu
NM_001304717.5:c.1633_1635delinsGAA NP_001291646.4:p.Asn545Glu
NM_001304718.2:c.523_525delinsGAA NP_001291647.1:p.Asn175Glu
NM_000314.8:c.1114_1116delinsGAA MANE Select NP_000305.3:p.Asn372Glu