Canonical Allele Identifier: CA891837267
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965332_87965334delinsATT , CM000672.2:g.87965332_87965334delinsATT GRCh38
NC_000010.10:g.89725089_89725091delinsATT , CM000672.1:g.89725089_89725091delinsATT GRCh37
NC_000010.9:g.89715069_89715071delinsATT NCBI36
NG_007466.2:g.106894_106896delinsATT , LRG_311:g.106894_106896delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1165_1167delinsATT ENSP00000514759.2:p.Glu389Ile
ENST00000710265.1:c.*101_*103delinsATT ENSP00000518161.1:n.*101_*103delinsATT
ENST00000688158.2:n.1807_1809delinsATT
ENST00000688922.2:c.*902_*904delinsATT ENSP00000508742.2:n.*902_*904delinsATT
ENST00000700021.1:c.1027_1029delinsATT ENSP00000514757.1:p.Glu343Ile
ENST00000700022.1:c.*411_*413delinsATT ENSP00000514758.1:n.*411_*413delinsATT
ENST00000700023.1:n.2230_2232delinsATT
ENST00000700024.1:n.2464_2466delinsATT
ENST00000706954.1:c.1072_1074delinsATT ENSP00000516674.1:p.Glu358Ile
ENST00000706955.1:c.*1107_*1109delinsATT ENSP00000516675.1:n.*1107_*1109delinsATT
ENST00000686459.1:c.*658_*660delinsATT ENSP00000508909.1:n.*658_*660delinsATT
ENST00000688158.1:c.*1183_*1185delinsATT ENSP00000509254.1:n.*1183_*1185delinsATT
ENST00000688308.1:c.1072_1074delinsATT ENSP00000508752.1:p.Glu358Ile
ENST00000688922.1:c.993_995delinsATT
ENST00000693560.1:c.1591_1593delinsATT ENSP00000509861.1:p.Glu531Ile
ENST00000371953.8:c.1072_1074delinsATT MANE Select ENSP00000361021.3:p.Glu358Ile
ENST00000371953.7:c.1072_1074delinsATT ENSP00000361021.3:p.Glu358Ile
NM_000314.5:c.1072_1074delinsATT NP_000305.3:p.Glu358Ile
NM_000314.6:c.1072_1074delinsATT NP_000305.3:p.Glu358Ile
NM_001304717.2:c.1591_1593delinsATT NP_001291646.2:p.Glu531Ile
NM_001304718.1:c.481_483delinsATT NP_001291647.1:p.Glu161Ile
XM_006717926.2:c.1027_1029delinsATT XP_006717989.1:p.Glu343Ile
XM_011539982.1:c.976_978delinsATT XP_011538284.1:p.Glu326Ile
XR_945791.1:n.1642_1644delinsATT
NM_000314.7:c.1072_1074delinsATT NP_000305.3:p.Glu358Ile
NM_001304717.5:c.1591_1593delinsATT NP_001291646.4:p.Glu531Ile
NM_001304718.2:c.481_483delinsATT NP_001291647.1:p.Glu161Ile
NM_000314.8:c.1072_1074delinsATT MANE Select NP_000305.3:p.Glu358Ile