Canonical Allele Identifier: CA891837690
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965380_87965381delinsGT , CM000672.2:g.87965380_87965381delinsGT GRCh38
NC_000010.10:g.89725137_89725138delinsGT , CM000672.1:g.89725137_89725138delinsGT GRCh37
NC_000010.9:g.89715117_89715118delinsGT NCBI36
NG_007466.2:g.106942_106943delinsGT , LRG_311:g.106942_106943delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1213_1214delinsGT ENSP00000514759.2:p.Pro405Val
ENST00000710265.1:c.*149_*150delinsGT ENSP00000518161.1:n.*149_*150delinsGT
ENST00000688158.2:n.1855_1856delinsGT
ENST00000688922.2:c.*950_*951delinsGT ENSP00000508742.2:n.*950_*951delinsGT
ENST00000700021.1:c.1075_1076delinsGT ENSP00000514757.1:p.Pro359Val
ENST00000700022.1:c.*459_*460delinsGT ENSP00000514758.1:n.*459_*460delinsGT
ENST00000700023.1:n.2278_2279delinsGT
ENST00000700024.1:n.2512_2513delinsGT
ENST00000706954.1:c.1120_1121delinsGT ENSP00000516674.1:p.Pro374Val
ENST00000706955.1:c.*1155_*1156delinsGT ENSP00000516675.1:n.*1155_*1156delinsGT
ENST00000686459.1:c.*706_*707delinsGT ENSP00000508909.1:n.*706_*707delinsGT
ENST00000688158.1:c.*1231_*1232delinsGT ENSP00000509254.1:n.*1231_*1232delinsGT
ENST00000688308.1:c.1120_1121delinsGT ENSP00000508752.1:p.Pro374Val
ENST00000688922.1:c.1041_1042delinsGT
ENST00000693560.1:c.1639_1640delinsGT ENSP00000509861.1:p.Pro547Val
ENST00000371953.8:c.1120_1121delinsGT MANE Select ENSP00000361021.3:p.Pro374Val
ENST00000371953.7:c.1120_1121delinsGT ENSP00000361021.3:p.Pro374Val
NM_000314.5:c.1120_1121delinsGT NP_000305.3:p.Pro374Val
NM_000314.6:c.1120_1121delinsGT NP_000305.3:p.Pro374Val
NM_001304717.2:c.1639_1640delinsGT NP_001291646.2:p.Pro547Val
NM_001304718.1:c.529_530delinsGT NP_001291647.1:p.Pro177Val
XM_006717926.2:c.1075_1076delinsGT XP_006717989.1:p.Pro359Val
XM_011539982.1:c.1024_1025delinsGT XP_011538284.1:p.Pro342Val
XR_945791.1:n.1690_1691delinsGT
NM_000314.7:c.1120_1121delinsGT NP_000305.3:p.Pro374Val
NM_001304717.5:c.1639_1640delinsGT NP_001291646.4:p.Pro547Val
NM_001304718.2:c.529_530delinsGT NP_001291647.1:p.Pro177Val
NM_000314.8:c.1120_1121delinsGT MANE Select NP_000305.3:p.Pro374Val