Canonical Allele Identifier: CA891837353
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965341_87965343delinsGAA , CM000672.2:g.87965341_87965343delinsGAA GRCh38
NC_000010.10:g.89725098_89725100delinsGAA , CM000672.1:g.89725098_89725100delinsGAA GRCh37
NC_000010.9:g.89715078_89715080delinsGAA NCBI36
NG_007466.2:g.106903_106905delinsGAA , LRG_311:g.106903_106905delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1174_1176delinsGAA ENSP00000514759.2:p.Ser392Glu
ENST00000710265.1:c.*110_*112delinsGAA ENSP00000518161.1:n.*110_*112delinsGAA
ENST00000688158.2:n.1816_1818delinsGAA
ENST00000688922.2:c.*911_*913delinsGAA ENSP00000508742.2:n.*911_*913delinsGAA
ENST00000700021.1:c.1036_1038delinsGAA ENSP00000514757.1:p.Ser346Glu
ENST00000700022.1:c.*420_*422delinsGAA ENSP00000514758.1:n.*420_*422delinsGAA
ENST00000700023.1:n.2239_2241delinsGAA
ENST00000700024.1:n.2473_2475delinsGAA
ENST00000706954.1:c.1081_1083delinsGAA ENSP00000516674.1:p.Ser361Glu
ENST00000706955.1:c.*1116_*1118delinsGAA ENSP00000516675.1:n.*1116_*1118delinsGAA
ENST00000686459.1:c.*667_*669delinsGAA ENSP00000508909.1:n.*667_*669delinsGAA
ENST00000688158.1:c.*1192_*1194delinsGAA ENSP00000509254.1:n.*1192_*1194delinsGAA
ENST00000688308.1:c.1081_1083delinsGAA ENSP00000508752.1:p.Ser361Glu
ENST00000688922.1:c.1002_1004delinsGAA
ENST00000693560.1:c.1600_1602delinsGAA ENSP00000509861.1:p.Ser534Glu
ENST00000371953.8:c.1081_1083delinsGAA MANE Select ENSP00000361021.3:p.Ser361Glu
ENST00000371953.7:c.1081_1083delinsGAA ENSP00000361021.3:p.Ser361Glu
NM_000314.5:c.1081_1083delinsGAA NP_000305.3:p.Ser361Glu
NM_000314.6:c.1081_1083delinsGAA NP_000305.3:p.Ser361Glu
NM_001304717.2:c.1600_1602delinsGAA NP_001291646.2:p.Ser534Glu
NM_001304718.1:c.490_492delinsGAA NP_001291647.1:p.Ser164Glu
XM_006717926.2:c.1036_1038delinsGAA XP_006717989.1:p.Ser346Glu
XM_011539982.1:c.985_987delinsGAA XP_011538284.1:p.Ser329Glu
XR_945791.1:n.1651_1653delinsGAA
NM_000314.7:c.1081_1083delinsGAA NP_000305.3:p.Ser361Glu
NM_001304717.5:c.1600_1602delinsGAA NP_001291646.4:p.Ser534Glu
NM_001304718.2:c.490_492delinsGAA NP_001291647.1:p.Ser164Glu
NM_000314.8:c.1081_1083delinsGAA MANE Select NP_000305.3:p.Ser361Glu