Canonical Allele Identifier: CA891837655
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965377_87965379delinsCAT , CM000672.2:g.87965377_87965379delinsCAT GRCh38
NC_000010.10:g.89725134_89725136delinsCAT , CM000672.1:g.89725134_89725136delinsCAT GRCh37
NC_000010.9:g.89715114_89715116delinsCAT NCBI36
NG_007466.2:g.106939_106941delinsCAT , LRG_311:g.106939_106941delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1210_1212delinsCAT ENSP00000514759.2:p.Glu404His
ENST00000710265.1:c.*146_*148delinsCAT ENSP00000518161.1:n.*146_*148delinsCAT
ENST00000688158.2:n.1852_1854delinsCAT
ENST00000688922.2:c.*947_*949delinsCAT ENSP00000508742.2:n.*947_*949delinsCAT
ENST00000700021.1:c.1072_1074delinsCAT ENSP00000514757.1:p.Glu358His
ENST00000700022.1:c.*456_*458delinsCAT ENSP00000514758.1:n.*456_*458delinsCAT
ENST00000700023.1:n.2275_2277delinsCAT
ENST00000700024.1:n.2509_2511delinsCAT
ENST00000706954.1:c.1117_1119delinsCAT ENSP00000516674.1:p.Glu373His
ENST00000706955.1:c.*1152_*1154delinsCAT ENSP00000516675.1:n.*1152_*1154delinsCAT
ENST00000686459.1:c.*703_*705delinsCAT ENSP00000508909.1:n.*703_*705delinsCAT
ENST00000688158.1:c.*1228_*1230delinsCAT ENSP00000509254.1:n.*1228_*1230delinsCAT
ENST00000688308.1:c.1117_1119delinsCAT ENSP00000508752.1:p.Glu373His
ENST00000688922.1:c.1038_1040delinsCAT
ENST00000693560.1:c.1636_1638delinsCAT ENSP00000509861.1:p.Glu546His
ENST00000371953.8:c.1117_1119delinsCAT MANE Select ENSP00000361021.3:p.Glu373His
ENST00000371953.7:c.1117_1119delinsCAT ENSP00000361021.3:p.Glu373His
NM_000314.5:c.1117_1119delinsCAT NP_000305.3:p.Glu373His
NM_000314.6:c.1117_1119delinsCAT NP_000305.3:p.Glu373His
NM_001304717.2:c.1636_1638delinsCAT NP_001291646.2:p.Glu546His
NM_001304718.1:c.526_528delinsCAT NP_001291647.1:p.Glu176His
XM_006717926.2:c.1072_1074delinsCAT XP_006717989.1:p.Glu358His
XM_011539982.1:c.1021_1023delinsCAT XP_011538284.1:p.Glu341His
XR_945791.1:n.1687_1689delinsCAT
NM_000314.7:c.1117_1119delinsCAT NP_000305.3:p.Glu373His
NM_001304717.5:c.1636_1638delinsCAT NP_001291646.4:p.Glu546His
NM_001304718.2:c.526_528delinsCAT NP_001291647.1:p.Glu176His
NM_000314.8:c.1117_1119delinsCAT MANE Select NP_000305.3:p.Glu373His