Canonical Allele Identifier: CA891835164
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894076_87894077delinsCT , CM000672.2:g.87894076_87894077delinsCT GRCh38
NC_000010.10:g.89653833_89653834delinsCT , CM000672.1:g.89653833_89653834delinsCT GRCh37
NC_000010.9:g.89643813_89643814delinsCT NCBI36
NG_007466.2:g.35638_35639delinsCT , LRG_311:g.35638_35639delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.131_132delinsCT ENSP00000514759.2:p.Gly44Ala
ENST00000710265.1:c.131_132delinsCT ENSP00000518161.1:p.Gly44Ala
ENST00000472832.3:c.131_132delinsCT ENSP00000483066.2:p.Gly44Ala
ENST00000688158.2:n.899+13638_899+13639delinsCT
ENST00000688922.2:c.131_132delinsCT ENSP00000508742.2:p.Gly44Ala
ENST00000700021.1:c.131_132delinsCT ENSP00000514757.1:p.Gly44Ala
ENST00000700022.1:c.131_132delinsCT ENSP00000514758.1:p.Gly44Ala
ENST00000706954.1:c.131_132delinsCT ENSP00000516674.1:p.Gly44Ala
ENST00000706955.1:c.*166_*167delinsCT ENSP00000516675.1:n.*166_*167delinsCT
ENST00000686459.1:c.131_132delinsCT ENSP00000508909.1:p.Gly44Ala
ENST00000688158.1:c.*275+13638_*275+13639delinsCT ENSP00000509254.1:n.*275+13638_*275+13639delinsCT
ENST00000688308.1:c.131_132delinsCT ENSP00000508752.1:p.Gly44Ala
ENST00000693560.1:c.650_651delinsCT ENSP00000509861.1:p.Gly217Ala
ENST00000371953.8:c.131_132delinsCT MANE Select ENSP00000361021.3:p.Gly44Ala
ENST00000371953.7:c.131_132delinsCT ENSP00000361021.3:p.Gly44Ala
ENST00000462694.1:n.133_134delinsCT
ENST00000610634.1:c.29_30delinsCT ENSP00000477517.1:p.Gly10Ala
NM_000314.5:c.131_132delinsCT NP_000305.3:p.Gly44Ala
NM_000314.6:c.131_132delinsCT NP_000305.3:p.Gly44Ala
NM_001304717.2:c.650_651delinsCT NP_001291646.2:p.Gly217Ala
NM_001304718.1:c.-575_-574delinsCT NP_001291647.1:n.-575_-574delinsCT
XM_006717926.2:c.131_132delinsCT XP_006717989.1:p.Gly44Ala
XM_011539981.1:c.131_132delinsCT XP_011538283.1:p.Gly44Ala
XM_011539982.1:c.68+13638_68+13639delinsCT XP_011538284.1:n.68+13638_68+13639delinsCT
XR_945789.1:n.843_844delinsCT
XR_945790.1:n.843_844delinsCT
XR_945791.1:n.843_844delinsCT
NM_000314.7:c.131_132delinsCT NP_000305.3:p.Gly44Ala
NM_001304717.5:c.650_651delinsCT NP_001291646.4:p.Gly217Ala
NM_001304718.2:c.-575_-574delinsCT NP_001291647.1:n.-575_-574delinsCT
NM_000314.8:c.131_132delinsCT MANE Select NP_000305.3:p.Gly44Ala