Canonical Allele Identifier: CA891835956
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961005_87961007delinsGAA , CM000672.2:g.87961005_87961007delinsGAA GRCh38
NC_000010.10:g.89720762_89720764delinsGAA , CM000672.1:g.89720762_89720764delinsGAA GRCh37
NC_000010.9:g.89710742_89710744delinsGAA NCBI36
NG_007466.2:g.102567_102569delinsGAA , LRG_311:g.102567_102569delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1006_1008delinsGAA ENSP00000514759.2:p.Ser336Glu
ENST00000710265.1:c.913_915delinsGAA ENSP00000518161.1:p.Ser305Glu
ENST00000472832.3:c.913_915delinsGAA ENSP00000483066.2:p.Ser305Glu
ENST00000688158.2:n.1648_1650delinsGAA
ENST00000688922.2:c.*743_*745delinsGAA ENSP00000508742.2:n.*743_*745delinsGAA
ENST00000700021.1:c.868_870delinsGAA ENSP00000514757.1:p.Ser290Glu
ENST00000700022.1:c.*252_*254delinsGAA ENSP00000514758.1:n.*252_*254delinsGAA
ENST00000700023.1:n.2071_2073delinsGAA
ENST00000700024.1:n.2305_2307delinsGAA
ENST00000700025.1:n.1682_1684delinsGAA
ENST00000700026.1:n.550_552delinsGAA
ENST00000706954.1:c.913_915delinsGAA ENSP00000516674.1:p.Ser305Glu
ENST00000706955.1:c.*948_*950delinsGAA ENSP00000516675.1:n.*948_*950delinsGAA
ENST00000686459.1:c.*499_*501delinsGAA ENSP00000508909.1:n.*499_*501delinsGAA
ENST00000688158.1:c.*1024_*1026delinsGAA ENSP00000509254.1:n.*1024_*1026delinsGAA
ENST00000688308.1:c.913_915delinsGAA ENSP00000508752.1:p.Ser305Glu
ENST00000688922.1:c.834_836delinsGAA
ENST00000693560.1:c.1432_1434delinsGAA ENSP00000509861.1:p.Ser478Glu
ENST00000371953.8:c.913_915delinsGAA MANE Select ENSP00000361021.3:p.Ser305Glu
ENST00000371953.7:c.913_915delinsGAA ENSP00000361021.3:p.Ser305Glu
ENST00000472832.2:c.340_342delinsGAA ENSP00000483066.1:p.Ser114Glu
NM_000314.5:c.913_915delinsGAA NP_000305.3:p.Ser305Glu
NM_000314.6:c.913_915delinsGAA NP_000305.3:p.Ser305Glu
NM_001304717.2:c.1432_1434delinsGAA NP_001291646.2:p.Ser478Glu
NM_001304718.1:c.322_324delinsGAA NP_001291647.1:p.Ser108Glu
XM_006717926.2:c.868_870delinsGAA XP_006717989.1:p.Ser290Glu
XM_011539981.1:c.913_915delinsGAA XP_011538283.1:p.Ser305Glu
XM_011539982.1:c.817_819delinsGAA XP_011538284.1:p.Ser273Glu
XR_945791.1:n.1483_1485delinsGAA
NM_000314.7:c.913_915delinsGAA NP_000305.3:p.Ser305Glu
NM_001304717.5:c.1432_1434delinsGAA NP_001291646.4:p.Ser478Glu
NM_001304718.2:c.322_324delinsGAA NP_001291647.1:p.Ser108Glu
NM_000314.8:c.913_915delinsGAA MANE Select NP_000305.3:p.Ser305Glu