Canonical Allele Identifier: CA891837444
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933129_87933131delinsAGA , CM000672.2:g.87933129_87933131delinsAGA GRCh38
NC_000010.10:g.89692886_89692888delinsAGA , CM000672.1:g.89692886_89692888delinsAGA GRCh37
NC_000010.9:g.89682866_89682868delinsAGA NCBI36
NG_007466.2:g.74691_74693delinsAGA , LRG_311:g.74691_74693delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.370_372delinsAGA ENSP00000514759.2:p.Cys124Arg
ENST00000710265.1:c.370_372delinsAGA ENSP00000518161.1:p.Cys124Arg
ENST00000472832.3:c.370_372delinsAGA ENSP00000483066.2:p.Cys124Arg
ENST00000688158.2:n.1105_1107delinsAGA
ENST00000688922.2:c.*200_*202delinsAGA ENSP00000508742.2:n.*200_*202delinsAGA
ENST00000700021.1:c.325_327delinsAGA ENSP00000514757.1:p.Cys109Arg
ENST00000700022.1:c.370_372delinsAGA ENSP00000514758.1:p.Cys124Arg
ENST00000700029.1:c.204_206delinsAGA
ENST00000706954.1:c.370_372delinsAGA ENSP00000516674.1:p.Cys124Arg
ENST00000706955.1:c.*405_*407delinsAGA ENSP00000516675.1:n.*405_*407delinsAGA
ENST00000686459.1:c.370_372delinsAGA ENSP00000508909.1:p.Cys124Arg
ENST00000688158.1:c.*481_*483delinsAGA ENSP00000509254.1:n.*481_*483delinsAGA
ENST00000688308.1:c.370_372delinsAGA ENSP00000508752.1:p.Cys124Arg
ENST00000688922.1:c.291_293delinsAGA
ENST00000693560.1:c.889_891delinsAGA ENSP00000509861.1:p.Cys297Arg
ENST00000371953.8:c.370_372delinsAGA MANE Select ENSP00000361021.3:p.Cys124Arg
ENST00000371953.7:c.370_372delinsAGA ENSP00000361021.3:p.Cys124Arg
ENST00000498703.1:n.196_198delinsAGA
ENST00000610634.1:c.268_270delinsAGA ENSP00000477517.1:p.Cys90Arg
NM_000314.5:c.370_372delinsAGA NP_000305.3:p.Cys124Arg
NM_000314.6:c.370_372delinsAGA NP_000305.3:p.Cys124Arg
NM_001304717.2:c.889_891delinsAGA NP_001291646.2:p.Cys297Arg
NM_001304718.1:c.-381_-379delinsAGA NP_001291647.1:n.-381_-379delinsAGA
XM_006717926.2:c.325_327delinsAGA XP_006717989.1:p.Cys109Arg
XM_011539981.1:c.370_372delinsAGA XP_011538283.1:p.Cys124Arg
XM_011539982.1:c.274_276delinsAGA XP_011538284.1:p.Cys92Arg
XR_945789.1:n.1082_1084delinsAGA
XR_945790.1:n.1082_1084delinsAGA
XR_945791.1:n.1082_1084delinsAGA
NM_000314.7:c.370_372delinsAGA NP_000305.3:p.Cys124Arg
NM_001304717.5:c.889_891delinsAGA NP_001291646.4:p.Cys297Arg
NM_001304718.2:c.-381_-379delinsAGA NP_001291647.1:n.-381_-379delinsAGA
NM_000314.8:c.370_372delinsAGA MANE Select NP_000305.3:p.Cys124Arg