Canonical Allele Identifier: CA891837630
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965376delinsCAA , CM000672.2:g.87965374_87965376delinsCAA GRCh38
NC_000010.10:g.89725131_89725133delinsCAA , CM000672.1:g.89725131_89725133delinsCAA GRCh37
NC_000010.9:g.89715111_89715113delinsCAA NCBI36
NG_007466.2:g.106936_106938delinsCAA , LRG_311:g.106936_106938delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1209delinsCAA ENSP00000514759.2:p.Asn403Gln
ENST00000710265.1:c.*143_*145delinsCAA ENSP00000518161.1:n.*143_*145delinsCAA
ENST00000688158.2:n.1849_1851delinsCAA
ENST00000688922.2:c.*944_*946delinsCAA ENSP00000508742.2:n.*944_*946delinsCAA
ENST00000700021.1:c.1069_1071delinsCAA ENSP00000514757.1:p.Asn357Gln
ENST00000700022.1:c.*453_*455delinsCAA ENSP00000514758.1:n.*453_*455delinsCAA
ENST00000700023.1:n.2272_2274delinsCAA
ENST00000700024.1:n.2506_2508delinsCAA
ENST00000706954.1:c.1114_1116delinsCAA ENSP00000516674.1:p.Asn372Gln
ENST00000706955.1:c.*1149_*1151delinsCAA ENSP00000516675.1:n.*1149_*1151delinsCAA
ENST00000686459.1:c.*700_*702delinsCAA ENSP00000508909.1:n.*700_*702delinsCAA
ENST00000688158.1:c.*1225_*1227delinsCAA ENSP00000509254.1:n.*1225_*1227delinsCAA
ENST00000688308.1:c.1114_1116delinsCAA ENSP00000508752.1:p.Asn372Gln
ENST00000688922.1:c.1035_1037delinsCAA
ENST00000693560.1:c.1633_1635delinsCAA ENSP00000509861.1:p.Asn545Gln
ENST00000371953.8:c.1114_1116delinsCAA MANE Select ENSP00000361021.3:p.Asn372Gln
ENST00000371953.7:c.1114_1116delinsCAA ENSP00000361021.3:p.Asn372Gln
NM_000314.5:c.1114_1116delinsCAA NP_000305.3:p.Asn372Gln
NM_000314.6:c.1114_1116delinsCAA NP_000305.3:p.Asn372Gln
NM_001304717.2:c.1633_1635delinsCAA NP_001291646.2:p.Asn545Gln
NM_001304718.1:c.523_525delinsCAA NP_001291647.1:p.Asn175Gln
XM_006717926.2:c.1069_1071delinsCAA XP_006717989.1:p.Asn357Gln
XM_011539982.1:c.1018_1020delinsCAA XP_011538284.1:p.Asn340Gln
XR_945791.1:n.1684_1686delinsCAA
NM_000314.7:c.1114_1116delinsCAA NP_000305.3:p.Asn372Gln
NM_001304717.5:c.1633_1635delinsCAA NP_001291646.4:p.Asn545Gln
NM_001304718.2:c.523_525delinsCAA NP_001291647.1:p.Asn175Gln
NM_000314.8:c.1114_1116delinsCAA MANE Select NP_000305.3:p.Asn372Gln