Canonical Allele Identifier: CA891837712
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965383_87965384delinsTC , CM000672.2:g.87965383_87965384delinsTC GRCh38
NC_000010.10:g.89725140_89725141delinsTC , CM000672.1:g.89725140_89725141delinsTC GRCh37
NC_000010.9:g.89715120_89715121delinsTC NCBI36
NG_007466.2:g.106945_106946delinsTC , LRG_311:g.106945_106946delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1216_1217delinsTC ENSP00000514759.2:p.Asp406Ser
ENST00000710265.1:c.*152_*153delinsTC ENSP00000518161.1:n.*152_*153delinsTC
ENST00000688158.2:n.1858_1859delinsTC
ENST00000688922.2:c.*953_*954delinsTC ENSP00000508742.2:n.*953_*954delinsTC
ENST00000700021.1:c.1078_1079delinsTC ENSP00000514757.1:p.Asp360Ser
ENST00000700022.1:c.*462_*463delinsTC ENSP00000514758.1:n.*462_*463delinsTC
ENST00000700023.1:n.2281_2282delinsTC
ENST00000700024.1:n.2515_2516delinsTC
ENST00000706954.1:c.1123_1124delinsTC ENSP00000516674.1:p.Asp375Ser
ENST00000706955.1:c.*1158_*1159delinsTC ENSP00000516675.1:n.*1158_*1159delinsTC
ENST00000686459.1:c.*709_*710delinsTC ENSP00000508909.1:n.*709_*710delinsTC
ENST00000688158.1:c.*1234_*1235delinsTC ENSP00000509254.1:n.*1234_*1235delinsTC
ENST00000688308.1:c.1123_1124delinsTC ENSP00000508752.1:p.Asp375Ser
ENST00000688922.1:c.1044_1045delinsTC
ENST00000693560.1:c.1642_1643delinsTC ENSP00000509861.1:p.Asp548Ser
ENST00000371953.8:c.1123_1124delinsTC MANE Select ENSP00000361021.3:p.Asp375Ser
ENST00000371953.7:c.1123_1124delinsTC ENSP00000361021.3:p.Asp375Ser
NM_000314.5:c.1123_1124delinsTC NP_000305.3:p.Asp375Ser
NM_000314.6:c.1123_1124delinsTC NP_000305.3:p.Asp375Ser
NM_001304717.2:c.1642_1643delinsTC NP_001291646.2:p.Asp548Ser
NM_001304718.1:c.532_533delinsTC NP_001291647.1:p.Asp178Ser
XM_006717926.2:c.1078_1079delinsTC XP_006717989.1:p.Asp360Ser
XM_011539982.1:c.1027_1028delinsTC XP_011538284.1:p.Asp343Ser
XR_945791.1:n.1693_1694delinsTC
NM_000314.7:c.1123_1124delinsTC NP_000305.3:p.Asp375Ser
NM_001304717.5:c.1642_1643delinsTC NP_001291646.4:p.Asp548Ser
NM_001304718.2:c.532_533delinsTC NP_001291647.1:p.Asp178Ser
NM_000314.8:c.1123_1124delinsTC MANE Select NP_000305.3:p.Asp375Ser