Canonical Allele Identifier: CA891841622
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965383_87965384delinsCC , CM000672.2:g.87965383_87965384delinsCC GRCh38
NC_000010.10:g.89725140_89725141delinsCC , CM000672.1:g.89725140_89725141delinsCC GRCh37
NC_000010.9:g.89715120_89715121delinsCC NCBI36
NG_007466.2:g.106945_106946delinsCC , LRG_311:g.106945_106946delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1216_1217delinsCC ENSP00000514759.2:p.Asp406Pro
ENST00000710265.1:c.*152_*153delinsCC ENSP00000518161.1:n.*152_*153delinsCC
ENST00000688158.2:n.1858_1859delinsCC
ENST00000688922.2:c.*953_*954delinsCC ENSP00000508742.2:n.*953_*954delinsCC
ENST00000700021.1:c.1078_1079delinsCC ENSP00000514757.1:p.Asp360Pro
ENST00000700022.1:c.*462_*463delinsCC ENSP00000514758.1:n.*462_*463delinsCC
ENST00000700023.1:n.2281_2282delinsCC
ENST00000700024.1:n.2515_2516delinsCC
ENST00000706954.1:c.1123_1124delinsCC ENSP00000516674.1:p.Asp375Pro
ENST00000706955.1:c.*1158_*1159delinsCC ENSP00000516675.1:n.*1158_*1159delinsCC
ENST00000686459.1:c.*709_*710delinsCC ENSP00000508909.1:n.*709_*710delinsCC
ENST00000688158.1:c.*1234_*1235delinsCC ENSP00000509254.1:n.*1234_*1235delinsCC
ENST00000688308.1:c.1123_1124delinsCC ENSP00000508752.1:p.Asp375Pro
ENST00000688922.1:c.1044_1045delinsCC
ENST00000693560.1:c.1642_1643delinsCC ENSP00000509861.1:p.Asp548Pro
ENST00000371953.8:c.1123_1124delinsCC MANE Select ENSP00000361021.3:p.Asp375Pro
ENST00000371953.7:c.1123_1124delinsCC ENSP00000361021.3:p.Asp375Pro
NM_000314.5:c.1123_1124delinsCC NP_000305.3:p.Asp375Pro
NM_000314.6:c.1123_1124delinsCC NP_000305.3:p.Asp375Pro
NM_001304717.2:c.1642_1643delinsCC NP_001291646.2:p.Asp548Pro
NM_001304718.1:c.532_533delinsCC NP_001291647.1:p.Asp178Pro
XM_006717926.2:c.1078_1079delinsCC XP_006717989.1:p.Asp360Pro
XM_011539982.1:c.1027_1028delinsCC XP_011538284.1:p.Asp343Pro
XR_945791.1:n.1693_1694delinsCC
NM_000314.7:c.1123_1124delinsCC NP_000305.3:p.Asp375Pro
NM_001304717.5:c.1642_1643delinsCC NP_001291646.4:p.Asp548Pro
NM_001304718.2:c.532_533delinsCC NP_001291647.1:p.Asp178Pro
NM_000314.8:c.1123_1124delinsCC MANE Select NP_000305.3:p.Asp375Pro