Canonical Allele Identifier: CA891837917
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933165_87933167delinsCCA , CM000672.2:g.87933165_87933167delinsCCA GRCh38
NC_000010.10:g.89692922_89692924delinsCCA , CM000672.1:g.89692922_89692924delinsCCA GRCh37
NC_000010.9:g.89682902_89682904delinsCCA NCBI36
NG_007466.2:g.74727_74729delinsCCA , LRG_311:g.74727_74729delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.406_408delinsCCA ENSP00000514759.2:p.Cys136Pro
ENST00000710265.1:c.406_408delinsCCA ENSP00000518161.1:p.Cys136Pro
ENST00000472832.3:c.406_408delinsCCA ENSP00000483066.2:p.Cys136Pro
ENST00000688158.2:n.1141_1143delinsCCA
ENST00000688922.2:c.*236_*238delinsCCA ENSP00000508742.2:n.*236_*238delinsCCA
ENST00000700021.1:c.361_363delinsCCA ENSP00000514757.1:p.Cys121Pro
ENST00000700022.1:c.406_408delinsCCA ENSP00000514758.1:p.Cys136Pro
ENST00000700029.1:c.240_242delinsCCA
ENST00000706954.1:c.406_408delinsCCA ENSP00000516674.1:p.Cys136Pro
ENST00000706955.1:c.*441_*443delinsCCA ENSP00000516675.1:n.*441_*443delinsCCA
ENST00000686459.1:c.406_408delinsCCA ENSP00000508909.1:p.Cys136Pro
ENST00000688158.1:c.*517_*519delinsCCA ENSP00000509254.1:n.*517_*519delinsCCA
ENST00000688308.1:c.406_408delinsCCA ENSP00000508752.1:p.Cys136Pro
ENST00000688922.1:c.327_329delinsCCA
ENST00000693560.1:c.925_927delinsCCA ENSP00000509861.1:p.Cys309Pro
ENST00000371953.8:c.406_408delinsCCA MANE Select ENSP00000361021.3:p.Cys136Pro
ENST00000371953.7:c.406_408delinsCCA ENSP00000361021.3:p.Cys136Pro
ENST00000498703.1:n.232_234delinsCCA
ENST00000610634.1:c.304_306delinsCCA ENSP00000477517.1:p.Cys102Pro
NM_000314.5:c.406_408delinsCCA NP_000305.3:p.Cys136Pro
NM_000314.6:c.406_408delinsCCA NP_000305.3:p.Cys136Pro
NM_001304717.2:c.925_927delinsCCA NP_001291646.2:p.Cys309Pro
NM_001304718.1:c.-345_-343delinsCCA NP_001291647.1:n.-345_-343delinsCCA
XM_006717926.2:c.361_363delinsCCA XP_006717989.1:p.Cys121Pro
XM_011539981.1:c.406_408delinsCCA XP_011538283.1:p.Cys136Pro
XM_011539982.1:c.310_312delinsCCA XP_011538284.1:p.Cys104Pro
XR_945789.1:n.1118_1120delinsCCA
XR_945790.1:n.1118_1120delinsCCA
XR_945791.1:n.1118_1120delinsCCA
NM_000314.7:c.406_408delinsCCA NP_000305.3:p.Cys136Pro
NM_001304717.5:c.925_927delinsCCA NP_001291646.4:p.Cys309Pro
NM_001304718.2:c.-345_-343delinsCCA NP_001291647.1:n.-345_-343delinsCCA
NM_000314.8:c.406_408delinsCCA MANE Select NP_000305.3:p.Cys136Pro