Canonical Allele Identifier: CA891839780
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957946_87957947delinsGG , CM000672.2:g.87957946_87957947delinsGG GRCh38
NC_000010.10:g.89717703_89717704delinsGG , CM000672.1:g.89717703_89717704delinsGG GRCh37
NC_000010.9:g.89707683_89707684delinsGG NCBI36
NG_007466.2:g.99508_99509delinsGG , LRG_311:g.99508_99509delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.728_729delinsGG ENSP00000514759.2:p.Phe243Trp
ENST00000710265.1:c.728_729delinsGG ENSP00000518161.1:p.Phe243Trp
ENST00000472832.3:c.728_729delinsGG ENSP00000483066.2:p.Phe243Trp
ENST00000688158.2:n.1463_1464delinsGG
ENST00000688922.2:c.*558_*559delinsGG ENSP00000508742.2:n.*558_*559delinsGG
ENST00000700021.1:c.683_684delinsGG ENSP00000514757.1:p.Phe228Trp
ENST00000700022.1:c.*67_*68delinsGG ENSP00000514758.1:n.*67_*68delinsGG
ENST00000700023.1:n.1886_1887delinsGG
ENST00000700024.1:n.2120_2121delinsGG
ENST00000700025.1:n.1497_1498delinsGG
ENST00000700026.1:n.365_366delinsGG
ENST00000700029.1:c.562_563delinsGG
ENST00000706954.1:c.728_729delinsGG ENSP00000516674.1:p.Phe243Trp
ENST00000706955.1:c.*763_*764delinsGG ENSP00000516675.1:n.*763_*764delinsGG
ENST00000686459.1:c.*314_*315delinsGG ENSP00000508909.1:n.*314_*315delinsGG
ENST00000688158.1:c.*839_*840delinsGG ENSP00000509254.1:n.*839_*840delinsGG
ENST00000688308.1:c.728_729delinsGG ENSP00000508752.1:p.Phe243Trp
ENST00000688922.1:c.649_650delinsGG
ENST00000693560.1:c.1247_1248delinsGG ENSP00000509861.1:p.Phe416Trp
ENST00000371953.8:c.728_729delinsGG MANE Select ENSP00000361021.3:p.Phe243Trp
ENST00000371953.7:c.728_729delinsGG ENSP00000361021.3:p.Phe243Trp
ENST00000472832.2:c.155_156delinsGG ENSP00000483066.1:p.Phe52Trp
NM_000314.5:c.728_729delinsGG NP_000305.3:p.Phe243Trp
NM_000314.6:c.728_729delinsGG NP_000305.3:p.Phe243Trp
NM_001304717.2:c.1247_1248delinsGG NP_001291646.2:p.Phe416Trp
NM_001304718.1:c.137_138delinsGG NP_001291647.1:p.Phe46Trp
XM_006717926.2:c.683_684delinsGG XP_006717989.1:p.Phe228Trp
XM_011539981.1:c.728_729delinsGG XP_011538283.1:p.Phe243Trp
XM_011539982.1:c.632_633delinsGG XP_011538284.1:p.Phe211Trp
XR_945791.1:n.1298_1299delinsGG
NM_000314.7:c.728_729delinsGG NP_000305.3:p.Phe243Trp
NM_001304717.5:c.1247_1248delinsGG NP_001291646.4:p.Phe416Trp
NM_001304718.2:c.137_138delinsGG NP_001291647.1:p.Phe46Trp
NM_000314.8:c.728_729delinsGG MANE Select NP_000305.3:p.Phe243Trp