Canonical Allele Identifier: CA891837714
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965383_87965384delinsAT , CM000672.2:g.87965383_87965384delinsAT GRCh38
NC_000010.10:g.89725140_89725141delinsAT , CM000672.1:g.89725140_89725141delinsAT GRCh37
NC_000010.9:g.89715120_89715121delinsAT NCBI36
NG_007466.2:g.106945_106946delinsAT , LRG_311:g.106945_106946delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1216_1217delinsAT ENSP00000514759.2:p.Asp406Ile
ENST00000710265.1:c.*152_*153delinsAT ENSP00000518161.1:n.*152_*153delinsAT
ENST00000688158.2:n.1858_1859delinsAT
ENST00000688922.2:c.*953_*954delinsAT ENSP00000508742.2:n.*953_*954delinsAT
ENST00000700021.1:c.1078_1079delinsAT ENSP00000514757.1:p.Asp360Ile
ENST00000700022.1:c.*462_*463delinsAT ENSP00000514758.1:n.*462_*463delinsAT
ENST00000700023.1:n.2281_2282delinsAT
ENST00000700024.1:n.2515_2516delinsAT
ENST00000706954.1:c.1123_1124delinsAT ENSP00000516674.1:p.Asp375Ile
ENST00000706955.1:c.*1158_*1159delinsAT ENSP00000516675.1:n.*1158_*1159delinsAT
ENST00000686459.1:c.*709_*710delinsAT ENSP00000508909.1:n.*709_*710delinsAT
ENST00000688158.1:c.*1234_*1235delinsAT ENSP00000509254.1:n.*1234_*1235delinsAT
ENST00000688308.1:c.1123_1124delinsAT ENSP00000508752.1:p.Asp375Ile
ENST00000688922.1:c.1044_1045delinsAT
ENST00000693560.1:c.1642_1643delinsAT ENSP00000509861.1:p.Asp548Ile
ENST00000371953.8:c.1123_1124delinsAT MANE Select ENSP00000361021.3:p.Asp375Ile
ENST00000371953.7:c.1123_1124delinsAT ENSP00000361021.3:p.Asp375Ile
NM_000314.5:c.1123_1124delinsAT NP_000305.3:p.Asp375Ile
NM_000314.6:c.1123_1124delinsAT NP_000305.3:p.Asp375Ile
NM_001304717.2:c.1642_1643delinsAT NP_001291646.2:p.Asp548Ile
NM_001304718.1:c.532_533delinsAT NP_001291647.1:p.Asp178Ile
XM_006717926.2:c.1078_1079delinsAT XP_006717989.1:p.Asp360Ile
XM_011539982.1:c.1027_1028delinsAT XP_011538284.1:p.Asp343Ile
XR_945791.1:n.1693_1694delinsAT
NM_000314.7:c.1123_1124delinsAT NP_000305.3:p.Asp375Ile
NM_001304717.5:c.1642_1643delinsAT NP_001291646.4:p.Asp548Ile
NM_001304718.2:c.532_533delinsAT NP_001291647.1:p.Asp178Ile
NM_000314.8:c.1123_1124delinsAT MANE Select NP_000305.3:p.Asp375Ile