Canonical Allele Identifier: CA891839778
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957946_87957947delinsAA , CM000672.2:g.87957946_87957947delinsAA GRCh38
NC_000010.10:g.89717703_89717704delinsAA , CM000672.1:g.89717703_89717704delinsAA GRCh37
NC_000010.9:g.89707683_89707684delinsAA NCBI36
NG_007466.2:g.99508_99509delinsAA , LRG_311:g.99508_99509delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.728_729delinsAA ENSP00000514759.2:p.Phe243Ter
ENST00000710265.1:c.728_729delinsAA ENSP00000518161.1:p.Phe243Ter
ENST00000472832.3:c.728_729delinsAA ENSP00000483066.2:p.Phe243Ter
ENST00000688158.2:n.1463_1464delinsAA
ENST00000688922.2:c.*558_*559delinsAA ENSP00000508742.2:n.*558_*559delinsAA
ENST00000700021.1:c.683_684delinsAA ENSP00000514757.1:p.Phe228Ter
ENST00000700022.1:c.*67_*68delinsAA ENSP00000514758.1:n.*67_*68delinsAA
ENST00000700023.1:n.1886_1887delinsAA
ENST00000700024.1:n.2120_2121delinsAA
ENST00000700025.1:n.1497_1498delinsAA
ENST00000700026.1:n.365_366delinsAA
ENST00000700029.1:c.562_563delinsAA
ENST00000706954.1:c.728_729delinsAA ENSP00000516674.1:p.Phe243Ter
ENST00000706955.1:c.*763_*764delinsAA ENSP00000516675.1:n.*763_*764delinsAA
ENST00000686459.1:c.*314_*315delinsAA ENSP00000508909.1:n.*314_*315delinsAA
ENST00000688158.1:c.*839_*840delinsAA ENSP00000509254.1:n.*839_*840delinsAA
ENST00000688308.1:c.728_729delinsAA ENSP00000508752.1:p.Phe243Ter
ENST00000688922.1:c.649_650delinsAA
ENST00000693560.1:c.1247_1248delinsAA ENSP00000509861.1:p.Phe416Ter
ENST00000371953.8:c.728_729delinsAA MANE Select ENSP00000361021.3:p.Phe243Ter
ENST00000371953.7:c.728_729delinsAA ENSP00000361021.3:p.Phe243Ter
ENST00000472832.2:c.155_156delinsAA ENSP00000483066.1:p.Phe52Ter
NM_000314.5:c.728_729delinsAA NP_000305.3:p.Phe243Ter
NM_000314.6:c.728_729delinsAA NP_000305.3:p.Phe243Ter
NM_001304717.2:c.1247_1248delinsAA NP_001291646.2:p.Phe416Ter
NM_001304718.1:c.137_138delinsAA NP_001291647.1:p.Phe46Ter
XM_006717926.2:c.683_684delinsAA XP_006717989.1:p.Phe228Ter
XM_011539981.1:c.728_729delinsAA XP_011538283.1:p.Phe243Ter
XM_011539982.1:c.632_633delinsAA XP_011538284.1:p.Phe211Ter
XR_945791.1:n.1298_1299delinsAA
NM_000314.7:c.728_729delinsAA NP_000305.3:p.Phe243Ter
NM_001304717.5:c.1247_1248delinsAA NP_001291646.4:p.Phe416Ter
NM_001304718.2:c.137_138delinsAA NP_001291647.1:p.Phe46Ter
NM_000314.8:c.728_729delinsAA MANE Select NP_000305.3:p.Phe243Ter