Canonical Allele Identifier: CA891838022
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965423_87965424delinsCT , CM000672.2:g.87965423_87965424delinsCT GRCh38
NC_000010.10:g.89725180_89725181delinsCT , CM000672.1:g.89725180_89725181delinsCT GRCh37
NC_000010.9:g.89715160_89715161delinsCT NCBI36
NG_007466.2:g.106985_106986delinsCT , LRG_311:g.106985_106986delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1256_1257delinsCT ENSP00000514759.2:p.Glu419Ala
ENST00000710265.1:c.*192_*193delinsCT ENSP00000518161.1:n.*192_*193delinsCT
ENST00000688158.2:n.1898_1899delinsCT
ENST00000688922.2:c.*993_*994delinsCT ENSP00000508742.2:n.*993_*994delinsCT
ENST00000700021.1:c.1118_1119delinsCT ENSP00000514757.1:p.Glu373Ala
ENST00000700022.1:c.*502_*503delinsCT ENSP00000514758.1:n.*502_*503delinsCT
ENST00000700023.1:n.2321_2322delinsCT
ENST00000700024.1:n.2555_2556delinsCT
ENST00000706954.1:c.1163_1164delinsCT ENSP00000516674.1:p.Glu388Ala
ENST00000706955.1:c.*1198_*1199delinsCT ENSP00000516675.1:n.*1198_*1199delinsCT
ENST00000686459.1:c.*749_*750delinsCT ENSP00000508909.1:n.*749_*750delinsCT
ENST00000688158.1:c.*1274_*1275delinsCT ENSP00000509254.1:n.*1274_*1275delinsCT
ENST00000688308.1:c.1163_1164delinsCT ENSP00000508752.1:p.Glu388Ala
ENST00000688922.1:c.1084_1085delinsCT
ENST00000693560.1:c.1682_1683delinsCT ENSP00000509861.1:p.Glu561Ala
ENST00000371953.8:c.1163_1164delinsCT MANE Select ENSP00000361021.3:p.Glu388Ala
ENST00000371953.7:c.1163_1164delinsCT ENSP00000361021.3:p.Glu388Ala
NM_000314.5:c.1163_1164delinsCT NP_000305.3:p.Glu388Ala
NM_000314.6:c.1163_1164delinsCT NP_000305.3:p.Glu388Ala
NM_001304717.2:c.1682_1683delinsCT NP_001291646.2:p.Glu561Ala
NM_001304718.1:c.572_573delinsCT NP_001291647.1:p.Glu191Ala
XM_006717926.2:c.1118_1119delinsCT XP_006717989.1:p.Glu373Ala
XM_011539982.1:c.1067_1068delinsCT XP_011538284.1:p.Glu356Ala
XR_945791.1:n.1733_1734delinsCT
NM_000314.7:c.1163_1164delinsCT NP_000305.3:p.Glu388Ala
NM_001304717.5:c.1682_1683delinsCT NP_001291646.4:p.Glu561Ala
NM_001304718.2:c.572_573delinsCT NP_001291647.1:p.Glu191Ala
NM_000314.8:c.1163_1164delinsCT MANE Select NP_000305.3:p.Glu388Ala