Canonical Allele Identifier: CA891839807
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957951_87957953delinsATT , CM000672.2:g.87957951_87957953delinsATT GRCh38
NC_000010.10:g.89717708_89717710delinsATT , CM000672.1:g.89717708_89717710delinsATT GRCh37
NC_000010.9:g.89707688_89707690delinsATT NCBI36
NG_007466.2:g.99513_99515delinsATT , LRG_311:g.99513_99515delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.733_735delinsATT ENSP00000514759.2:p.Gln245Ile
ENST00000710265.1:c.733_735delinsATT ENSP00000518161.1:p.Gln245Ile
ENST00000472832.3:c.733_735delinsATT ENSP00000483066.2:p.Gln245Ile
ENST00000688158.2:n.1468_1470delinsATT
ENST00000688922.2:c.*563_*565delinsATT ENSP00000508742.2:n.*563_*565delinsATT
ENST00000700021.1:c.688_690delinsATT ENSP00000514757.1:p.Gln230Ile
ENST00000700022.1:c.*72_*74delinsATT ENSP00000514758.1:n.*72_*74delinsATT
ENST00000700023.1:n.1891_1893delinsATT
ENST00000700024.1:n.2125_2127delinsATT
ENST00000700025.1:n.1502_1504delinsATT
ENST00000700026.1:n.370_372delinsATT
ENST00000700029.1:c.567_569delinsATT
ENST00000706954.1:c.733_735delinsATT ENSP00000516674.1:p.Gln245Ile
ENST00000706955.1:c.*768_*770delinsATT ENSP00000516675.1:n.*768_*770delinsATT
ENST00000686459.1:c.*319_*321delinsATT ENSP00000508909.1:n.*319_*321delinsATT
ENST00000688158.1:c.*844_*846delinsATT ENSP00000509254.1:n.*844_*846delinsATT
ENST00000688308.1:c.733_735delinsATT ENSP00000508752.1:p.Gln245Ile
ENST00000688922.1:c.654_656delinsATT
ENST00000693560.1:c.1252_1254delinsATT ENSP00000509861.1:p.Gln418Ile
ENST00000371953.8:c.733_735delinsATT MANE Select ENSP00000361021.3:p.Gln245Ile
ENST00000371953.7:c.733_735delinsATT ENSP00000361021.3:p.Gln245Ile
ENST00000472832.2:c.160_162delinsATT ENSP00000483066.1:p.Gln54Ile
NM_000314.5:c.733_735delinsATT NP_000305.3:p.Gln245Ile
NM_000314.6:c.733_735delinsATT NP_000305.3:p.Gln245Ile
NM_001304717.2:c.1252_1254delinsATT NP_001291646.2:p.Gln418Ile
NM_001304718.1:c.142_144delinsATT NP_001291647.1:p.Gln48Ile
XM_006717926.2:c.688_690delinsATT XP_006717989.1:p.Gln230Ile
XM_011539981.1:c.733_735delinsATT XP_011538283.1:p.Gln245Ile
XM_011539982.1:c.637_639delinsATT XP_011538284.1:p.Gln213Ile
XR_945791.1:n.1303_1305delinsATT
NM_000314.7:c.733_735delinsATT NP_000305.3:p.Gln245Ile
NM_001304717.5:c.1252_1254delinsATT NP_001291646.4:p.Gln418Ile
NM_001304718.2:c.142_144delinsATT NP_001291647.1:p.Gln48Ile
NM_000314.8:c.733_735delinsATT MANE Select NP_000305.3:p.Gln245Ile