Canonical Allele Identifier: CA891840777
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957945_87957946delinsCC , CM000672.2:g.87957945_87957946delinsCC GRCh38
NC_000010.10:g.89717702_89717703delinsCC , CM000672.1:g.89717702_89717703delinsCC GRCh37
NC_000010.9:g.89707682_89707683delinsCC NCBI36
NG_007466.2:g.99507_99508delinsCC , LRG_311:g.99507_99508delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.727_728delinsCC ENSP00000514759.2:p.Phe243Pro
ENST00000710265.1:c.727_728delinsCC ENSP00000518161.1:p.Phe243Pro
ENST00000472832.3:c.727_728delinsCC ENSP00000483066.2:p.Phe243Pro
ENST00000688158.2:n.1462_1463delinsCC
ENST00000688922.2:c.*557_*558delinsCC ENSP00000508742.2:n.*557_*558delinsCC
ENST00000700021.1:c.682_683delinsCC ENSP00000514757.1:p.Phe228Pro
ENST00000700022.1:c.*66_*67delinsCC ENSP00000514758.1:n.*66_*67delinsCC
ENST00000700023.1:n.1885_1886delinsCC
ENST00000700024.1:n.2119_2120delinsCC
ENST00000700025.1:n.1496_1497delinsCC
ENST00000700026.1:n.364_365delinsCC
ENST00000700029.1:c.561_562delinsCC
ENST00000706954.1:c.727_728delinsCC ENSP00000516674.1:p.Phe243Pro
ENST00000706955.1:c.*762_*763delinsCC ENSP00000516675.1:n.*762_*763delinsCC
ENST00000686459.1:c.*313_*314delinsCC ENSP00000508909.1:n.*313_*314delinsCC
ENST00000688158.1:c.*838_*839delinsCC ENSP00000509254.1:n.*838_*839delinsCC
ENST00000688308.1:c.727_728delinsCC ENSP00000508752.1:p.Phe243Pro
ENST00000688922.1:c.648_649delinsCC
ENST00000693560.1:c.1246_1247delinsCC ENSP00000509861.1:p.Phe416Pro
ENST00000371953.8:c.727_728delinsCC MANE Select ENSP00000361021.3:p.Phe243Pro
ENST00000371953.7:c.727_728delinsCC ENSP00000361021.3:p.Phe243Pro
ENST00000472832.2:c.154_155delinsCC ENSP00000483066.1:p.Phe52Pro
NM_000314.5:c.727_728delinsCC NP_000305.3:p.Phe243Pro
NM_000314.6:c.727_728delinsCC NP_000305.3:p.Phe243Pro
NM_001304717.2:c.1246_1247delinsCC NP_001291646.2:p.Phe416Pro
NM_001304718.1:c.136_137delinsCC NP_001291647.1:p.Phe46Pro
XM_006717926.2:c.682_683delinsCC XP_006717989.1:p.Phe228Pro
XM_011539981.1:c.727_728delinsCC XP_011538283.1:p.Phe243Pro
XM_011539982.1:c.631_632delinsCC XP_011538284.1:p.Phe211Pro
XR_945791.1:n.1297_1298delinsCC
NM_000314.7:c.727_728delinsCC NP_000305.3:p.Phe243Pro
NM_001304717.5:c.1246_1247delinsCC NP_001291646.4:p.Phe416Pro
NM_001304718.2:c.136_137delinsCC NP_001291647.1:p.Phe46Pro
NM_000314.8:c.727_728delinsCC MANE Select NP_000305.3:p.Phe243Pro