Canonical Allele Identifier: CA891839781
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957946_87957947delinsGT , CM000672.2:g.87957946_87957947delinsGT GRCh38
NC_000010.10:g.89717703_89717704delinsGT , CM000672.1:g.89717703_89717704delinsGT GRCh37
NC_000010.9:g.89707683_89707684delinsGT NCBI36
NG_007466.2:g.99508_99509delinsGT , LRG_311:g.99508_99509delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.728_729delinsGT ENSP00000514759.2:p.Phe243Cys
ENST00000710265.1:c.728_729delinsGT ENSP00000518161.1:p.Phe243Cys
ENST00000472832.3:c.728_729delinsGT ENSP00000483066.2:p.Phe243Cys
ENST00000688158.2:n.1463_1464delinsGT
ENST00000688922.2:c.*558_*559delinsGT ENSP00000508742.2:n.*558_*559delinsGT
ENST00000700021.1:c.683_684delinsGT ENSP00000514757.1:p.Phe228Cys
ENST00000700022.1:c.*67_*68delinsGT ENSP00000514758.1:n.*67_*68delinsGT
ENST00000700023.1:n.1886_1887delinsGT
ENST00000700024.1:n.2120_2121delinsGT
ENST00000700025.1:n.1497_1498delinsGT
ENST00000700026.1:n.365_366delinsGT
ENST00000700029.1:c.562_563delinsGT
ENST00000706954.1:c.728_729delinsGT ENSP00000516674.1:p.Phe243Cys
ENST00000706955.1:c.*763_*764delinsGT ENSP00000516675.1:n.*763_*764delinsGT
ENST00000686459.1:c.*314_*315delinsGT ENSP00000508909.1:n.*314_*315delinsGT
ENST00000688158.1:c.*839_*840delinsGT ENSP00000509254.1:n.*839_*840delinsGT
ENST00000688308.1:c.728_729delinsGT ENSP00000508752.1:p.Phe243Cys
ENST00000688922.1:c.649_650delinsGT
ENST00000693560.1:c.1247_1248delinsGT ENSP00000509861.1:p.Phe416Cys
ENST00000371953.8:c.728_729delinsGT MANE Select ENSP00000361021.3:p.Phe243Cys
ENST00000371953.7:c.728_729delinsGT ENSP00000361021.3:p.Phe243Cys
ENST00000472832.2:c.155_156delinsGT ENSP00000483066.1:p.Phe52Cys
NM_000314.5:c.728_729delinsGT NP_000305.3:p.Phe243Cys
NM_000314.6:c.728_729delinsGT NP_000305.3:p.Phe243Cys
NM_001304717.2:c.1247_1248delinsGT NP_001291646.2:p.Phe416Cys
NM_001304718.1:c.137_138delinsGT NP_001291647.1:p.Phe46Cys
XM_006717926.2:c.683_684delinsGT XP_006717989.1:p.Phe228Cys
XM_011539981.1:c.728_729delinsGT XP_011538283.1:p.Phe243Cys
XM_011539982.1:c.632_633delinsGT XP_011538284.1:p.Phe211Cys
XR_945791.1:n.1298_1299delinsGT
NM_000314.7:c.728_729delinsGT NP_000305.3:p.Phe243Cys
NM_001304717.5:c.1247_1248delinsGT NP_001291646.4:p.Phe416Cys
NM_001304718.2:c.137_138delinsGT NP_001291647.1:p.Phe46Cys
NM_000314.8:c.728_729delinsGT MANE Select NP_000305.3:p.Phe243Cys