Canonical Allele Identifier: CA891837703
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965380_87965381delinsTA , CM000672.2:g.87965380_87965381delinsTA GRCh38
NC_000010.10:g.89725137_89725138delinsTA , CM000672.1:g.89725137_89725138delinsTA GRCh37
NC_000010.9:g.89715117_89715118delinsTA NCBI36
NG_007466.2:g.106942_106943delinsTA , LRG_311:g.106942_106943delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1213_1214delinsTA ENSP00000514759.2:p.Pro405Tyr
ENST00000710265.1:c.*149_*150delinsTA ENSP00000518161.1:n.*149_*150delinsTA
ENST00000688158.2:n.1855_1856delinsTA
ENST00000688922.2:c.*950_*951delinsTA ENSP00000508742.2:n.*950_*951delinsTA
ENST00000700021.1:c.1075_1076delinsTA ENSP00000514757.1:p.Pro359Tyr
ENST00000700022.1:c.*459_*460delinsTA ENSP00000514758.1:n.*459_*460delinsTA
ENST00000700023.1:n.2278_2279delinsTA
ENST00000700024.1:n.2512_2513delinsTA
ENST00000706954.1:c.1120_1121delinsTA ENSP00000516674.1:p.Pro374Tyr
ENST00000706955.1:c.*1155_*1156delinsTA ENSP00000516675.1:n.*1155_*1156delinsTA
ENST00000686459.1:c.*706_*707delinsTA ENSP00000508909.1:n.*706_*707delinsTA
ENST00000688158.1:c.*1231_*1232delinsTA ENSP00000509254.1:n.*1231_*1232delinsTA
ENST00000688308.1:c.1120_1121delinsTA ENSP00000508752.1:p.Pro374Tyr
ENST00000688922.1:c.1041_1042delinsTA
ENST00000693560.1:c.1639_1640delinsTA ENSP00000509861.1:p.Pro547Tyr
ENST00000371953.8:c.1120_1121delinsTA MANE Select ENSP00000361021.3:p.Pro374Tyr
ENST00000371953.7:c.1120_1121delinsTA ENSP00000361021.3:p.Pro374Tyr
NM_000314.5:c.1120_1121delinsTA NP_000305.3:p.Pro374Tyr
NM_000314.6:c.1120_1121delinsTA NP_000305.3:p.Pro374Tyr
NM_001304717.2:c.1639_1640delinsTA NP_001291646.2:p.Pro547Tyr
NM_001304718.1:c.529_530delinsTA NP_001291647.1:p.Pro177Tyr
XM_006717926.2:c.1075_1076delinsTA XP_006717989.1:p.Pro359Tyr
XM_011539982.1:c.1024_1025delinsTA XP_011538284.1:p.Pro342Tyr
XR_945791.1:n.1690_1691delinsTA
NM_000314.7:c.1120_1121delinsTA NP_000305.3:p.Pro374Tyr
NM_001304717.5:c.1639_1640delinsTA NP_001291646.4:p.Pro547Tyr
NM_001304718.2:c.529_530delinsTA NP_001291647.1:p.Pro177Tyr
NM_000314.8:c.1120_1121delinsTA MANE Select NP_000305.3:p.Pro374Tyr