Canonical Allele Identifier: CA891837702
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965380_87965381delinsTT , CM000672.2:g.87965380_87965381delinsTT GRCh38
NC_000010.10:g.89725137_89725138delinsTT , CM000672.1:g.89725137_89725138delinsTT GRCh37
NC_000010.9:g.89715117_89715118delinsTT NCBI36
NG_007466.2:g.106942_106943delinsTT , LRG_311:g.106942_106943delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1213_1214delinsTT ENSP00000514759.2:p.Pro405Phe
ENST00000710265.1:c.*149_*150delinsTT ENSP00000518161.1:n.*149_*150delinsTT
ENST00000688158.2:n.1855_1856delinsTT
ENST00000688922.2:c.*950_*951delinsTT ENSP00000508742.2:n.*950_*951delinsTT
ENST00000700021.1:c.1075_1076delinsTT ENSP00000514757.1:p.Pro359Phe
ENST00000700022.1:c.*459_*460delinsTT ENSP00000514758.1:n.*459_*460delinsTT
ENST00000700023.1:n.2278_2279delinsTT
ENST00000700024.1:n.2512_2513delinsTT
ENST00000706954.1:c.1120_1121delinsTT ENSP00000516674.1:p.Pro374Phe
ENST00000706955.1:c.*1155_*1156delinsTT ENSP00000516675.1:n.*1155_*1156delinsTT
ENST00000686459.1:c.*706_*707delinsTT ENSP00000508909.1:n.*706_*707delinsTT
ENST00000688158.1:c.*1231_*1232delinsTT ENSP00000509254.1:n.*1231_*1232delinsTT
ENST00000688308.1:c.1120_1121delinsTT ENSP00000508752.1:p.Pro374Phe
ENST00000688922.1:c.1041_1042delinsTT
ENST00000693560.1:c.1639_1640delinsTT ENSP00000509861.1:p.Pro547Phe
ENST00000371953.8:c.1120_1121delinsTT MANE Select ENSP00000361021.3:p.Pro374Phe
ENST00000371953.7:c.1120_1121delinsTT ENSP00000361021.3:p.Pro374Phe
NM_000314.5:c.1120_1121delinsTT NP_000305.3:p.Pro374Phe
NM_000314.6:c.1120_1121delinsTT NP_000305.3:p.Pro374Phe
NM_001304717.2:c.1639_1640delinsTT NP_001291646.2:p.Pro547Phe
NM_001304718.1:c.529_530delinsTT NP_001291647.1:p.Pro177Phe
XM_006717926.2:c.1075_1076delinsTT XP_006717989.1:p.Pro359Phe
XM_011539982.1:c.1024_1025delinsTT XP_011538284.1:p.Pro342Phe
XR_945791.1:n.1690_1691delinsTT
NM_000314.7:c.1120_1121delinsTT NP_000305.3:p.Pro374Phe
NM_001304717.5:c.1639_1640delinsTT NP_001291646.4:p.Pro547Phe
NM_001304718.2:c.529_530delinsTT NP_001291647.1:p.Pro177Phe
NM_000314.8:c.1120_1121delinsTT MANE Select NP_000305.3:p.Pro374Phe