Canonical Allele Identifier: CA891837562
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933136_87933137delinsAA , CM000672.2:g.87933136_87933137delinsAA GRCh38
NC_000010.10:g.89692893_89692894delinsAA , CM000672.1:g.89692893_89692894delinsAA GRCh37
NC_000010.9:g.89682873_89682874delinsAA NCBI36
NG_007466.2:g.74698_74699delinsAA , LRG_311:g.74698_74699delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.377_378delinsAA ENSP00000514759.2:p.Ala126Glu
ENST00000710265.1:c.377_378delinsAA ENSP00000518161.1:p.Ala126Glu
ENST00000472832.3:c.377_378delinsAA ENSP00000483066.2:p.Ala126Glu
ENST00000688158.2:n.1112_1113delinsAA
ENST00000688922.2:c.*207_*208delinsAA ENSP00000508742.2:n.*207_*208delinsAA
ENST00000700021.1:c.332_333delinsAA ENSP00000514757.1:p.Ala111Glu
ENST00000700022.1:c.377_378delinsAA ENSP00000514758.1:p.Ala126Glu
ENST00000700029.1:c.211_212delinsAA
ENST00000706954.1:c.377_378delinsAA ENSP00000516674.1:p.Ala126Glu
ENST00000706955.1:c.*412_*413delinsAA ENSP00000516675.1:n.*412_*413delinsAA
ENST00000686459.1:c.377_378delinsAA ENSP00000508909.1:p.Ala126Glu
ENST00000688158.1:c.*488_*489delinsAA ENSP00000509254.1:n.*488_*489delinsAA
ENST00000688308.1:c.377_378delinsAA ENSP00000508752.1:p.Ala126Glu
ENST00000688922.1:c.298_299delinsAA
ENST00000693560.1:c.896_897delinsAA ENSP00000509861.1:p.Ala299Glu
ENST00000371953.8:c.377_378delinsAA MANE Select ENSP00000361021.3:p.Ala126Glu
ENST00000371953.7:c.377_378delinsAA ENSP00000361021.3:p.Ala126Glu
ENST00000498703.1:n.203_204delinsAA
ENST00000610634.1:c.275_276delinsAA ENSP00000477517.1:p.Ala92Glu
NM_000314.5:c.377_378delinsAA NP_000305.3:p.Ala126Glu
NM_000314.6:c.377_378delinsAA NP_000305.3:p.Ala126Glu
NM_001304717.2:c.896_897delinsAA NP_001291646.2:p.Ala299Glu
NM_001304718.1:c.-374_-373delinsAA NP_001291647.1:n.-374_-373delinsAA
XM_006717926.2:c.332_333delinsAA XP_006717989.1:p.Ala111Glu
XM_011539981.1:c.377_378delinsAA XP_011538283.1:p.Ala126Glu
XM_011539982.1:c.281_282delinsAA XP_011538284.1:p.Ala94Glu
XR_945789.1:n.1089_1090delinsAA
XR_945790.1:n.1089_1090delinsAA
XR_945791.1:n.1089_1090delinsAA
NM_000314.7:c.377_378delinsAA NP_000305.3:p.Ala126Glu
NM_001304717.5:c.896_897delinsAA NP_001291646.4:p.Ala299Glu
NM_001304718.2:c.-374_-373delinsAA NP_001291647.1:n.-374_-373delinsAA
NM_000314.8:c.377_378delinsAA MANE Select NP_000305.3:p.Ala126Glu