Canonical Allele Identifier: CA891841670
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965434_87965436delinsAAA , CM000672.2:g.87965434_87965436delinsAAA GRCh38
NC_000010.10:g.89725191_89725193delinsAAA , CM000672.1:g.89725191_89725193delinsAAA GRCh37
NC_000010.9:g.89715171_89715173delinsAAA NCBI36
NG_007466.2:g.106996_106998delinsAAA , LRG_311:g.106996_106998delinsAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1267_1269delinsAAA ENSP00000514759.2:p.Phe423Lys
ENST00000710265.1:c.*203_*205delinsAAA ENSP00000518161.1:n.*203_*205delinsAAA
ENST00000688158.2:n.1909_1911delinsAAA
ENST00000688922.2:c.*1004_*1006delinsAAA ENSP00000508742.2:n.*1004_*1006delinsAAA
ENST00000700021.1:c.1129_1131delinsAAA ENSP00000514757.1:p.Phe377Lys
ENST00000700022.1:c.*513_*515delinsAAA ENSP00000514758.1:n.*513_*515delinsAAA
ENST00000700023.1:n.2332_2334delinsAAA
ENST00000700024.1:n.2566_2568delinsAAA
ENST00000706954.1:c.1174_1176delinsAAA ENSP00000516674.1:p.Phe392Lys
ENST00000706955.1:c.*1209_*1211delinsAAA ENSP00000516675.1:n.*1209_*1211delinsAAA
ENST00000686459.1:c.*760_*762delinsAAA ENSP00000508909.1:n.*760_*762delinsAAA
ENST00000688158.1:c.*1285_*1287delinsAAA ENSP00000509254.1:n.*1285_*1287delinsAAA
ENST00000688308.1:c.1174_1176delinsAAA ENSP00000508752.1:p.Phe392Lys
ENST00000688922.1:c.1095_1097delinsAAA
ENST00000693560.1:c.1693_1695delinsAAA ENSP00000509861.1:p.Phe565Lys
ENST00000371953.8:c.1174_1176delinsAAA MANE Select ENSP00000361021.3:p.Phe392Lys
ENST00000371953.7:c.1174_1176delinsAAA ENSP00000361021.3:p.Phe392Lys
NM_000314.5:c.1174_1176delinsAAA NP_000305.3:p.Phe392Lys
NM_000314.6:c.1174_1176delinsAAA NP_000305.3:p.Phe392Lys
NM_001304717.2:c.1693_1695delinsAAA NP_001291646.2:p.Phe565Lys
NM_001304718.1:c.583_585delinsAAA NP_001291647.1:p.Phe195Lys
XM_006717926.2:c.1129_1131delinsAAA XP_006717989.1:p.Phe377Lys
XM_011539982.1:c.1078_1080delinsAAA XP_011538284.1:p.Phe360Lys
XR_945791.1:n.1744_1746delinsAAA
NM_000314.7:c.1174_1176delinsAAA NP_000305.3:p.Phe392Lys
NM_001304717.5:c.1693_1695delinsAAA NP_001291646.4:p.Phe565Lys
NM_001304718.2:c.583_585delinsAAA NP_001291647.1:p.Phe195Lys
NM_000314.8:c.1174_1176delinsAAA MANE Select NP_000305.3:p.Phe392Lys