Canonical Allele Identifier: CA891837541
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933135_87933137delinsCAA , CM000672.2:g.87933135_87933137delinsCAA GRCh38
NC_000010.10:g.89692892_89692894delinsCAA , CM000672.1:g.89692892_89692894delinsCAA GRCh37
NC_000010.9:g.89682872_89682874delinsCAA NCBI36
NG_007466.2:g.74697_74699delinsCAA , LRG_311:g.74697_74699delinsCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.376_378delinsCAA ENSP00000514759.2:p.Ala126Gln
ENST00000710265.1:c.376_378delinsCAA ENSP00000518161.1:p.Ala126Gln
ENST00000472832.3:c.376_378delinsCAA ENSP00000483066.2:p.Ala126Gln
ENST00000688158.2:n.1111_1113delinsCAA
ENST00000688922.2:c.*206_*208delinsCAA ENSP00000508742.2:n.*206_*208delinsCAA
ENST00000700021.1:c.331_333delinsCAA ENSP00000514757.1:p.Ala111Gln
ENST00000700022.1:c.376_378delinsCAA ENSP00000514758.1:p.Ala126Gln
ENST00000700029.1:c.210_212delinsCAA
ENST00000706954.1:c.376_378delinsCAA ENSP00000516674.1:p.Ala126Gln
ENST00000706955.1:c.*411_*413delinsCAA ENSP00000516675.1:n.*411_*413delinsCAA
ENST00000686459.1:c.376_378delinsCAA ENSP00000508909.1:p.Ala126Gln
ENST00000688158.1:c.*487_*489delinsCAA ENSP00000509254.1:n.*487_*489delinsCAA
ENST00000688308.1:c.376_378delinsCAA ENSP00000508752.1:p.Ala126Gln
ENST00000688922.1:c.297_299delinsCAA
ENST00000693560.1:c.895_897delinsCAA ENSP00000509861.1:p.Ala299Gln
ENST00000371953.8:c.376_378delinsCAA MANE Select ENSP00000361021.3:p.Ala126Gln
ENST00000371953.7:c.376_378delinsCAA ENSP00000361021.3:p.Ala126Gln
ENST00000498703.1:n.202_204delinsCAA
ENST00000610634.1:c.274_276delinsCAA ENSP00000477517.1:p.Ala92Gln
NM_000314.5:c.376_378delinsCAA NP_000305.3:p.Ala126Gln
NM_000314.6:c.376_378delinsCAA NP_000305.3:p.Ala126Gln
NM_001304717.2:c.895_897delinsCAA NP_001291646.2:p.Ala299Gln
NM_001304718.1:c.-375_-373delinsCAA NP_001291647.1:n.-375_-373delinsCAA
XM_006717926.2:c.331_333delinsCAA XP_006717989.1:p.Ala111Gln
XM_011539981.1:c.376_378delinsCAA XP_011538283.1:p.Ala126Gln
XM_011539982.1:c.280_282delinsCAA XP_011538284.1:p.Ala94Gln
XR_945789.1:n.1088_1090delinsCAA
XR_945790.1:n.1088_1090delinsCAA
XR_945791.1:n.1088_1090delinsCAA
NM_000314.7:c.376_378delinsCAA NP_000305.3:p.Ala126Gln
NM_001304717.5:c.895_897delinsCAA NP_001291646.4:p.Ala299Gln
NM_001304718.2:c.-375_-373delinsCAA NP_001291647.1:n.-375_-373delinsCAA
NM_000314.8:c.376_378delinsCAA MANE Select NP_000305.3:p.Ala126Gln