Canonical Allele Identifier: CA891837684
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965380_87965381delinsAA , CM000672.2:g.87965380_87965381delinsAA GRCh38
NC_000010.10:g.89725137_89725138delinsAA , CM000672.1:g.89725137_89725138delinsAA GRCh37
NC_000010.9:g.89715117_89715118delinsAA NCBI36
NG_007466.2:g.106942_106943delinsAA , LRG_311:g.106942_106943delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1213_1214delinsAA ENSP00000514759.2:p.Pro405Asn
ENST00000710265.1:c.*149_*150delinsAA ENSP00000518161.1:n.*149_*150delinsAA
ENST00000688158.2:n.1855_1856delinsAA
ENST00000688922.2:c.*950_*951delinsAA ENSP00000508742.2:n.*950_*951delinsAA
ENST00000700021.1:c.1075_1076delinsAA ENSP00000514757.1:p.Pro359Asn
ENST00000700022.1:c.*459_*460delinsAA ENSP00000514758.1:n.*459_*460delinsAA
ENST00000700023.1:n.2278_2279delinsAA
ENST00000700024.1:n.2512_2513delinsAA
ENST00000706954.1:c.1120_1121delinsAA ENSP00000516674.1:p.Pro374Asn
ENST00000706955.1:c.*1155_*1156delinsAA ENSP00000516675.1:n.*1155_*1156delinsAA
ENST00000686459.1:c.*706_*707delinsAA ENSP00000508909.1:n.*706_*707delinsAA
ENST00000688158.1:c.*1231_*1232delinsAA ENSP00000509254.1:n.*1231_*1232delinsAA
ENST00000688308.1:c.1120_1121delinsAA ENSP00000508752.1:p.Pro374Asn
ENST00000688922.1:c.1041_1042delinsAA
ENST00000693560.1:c.1639_1640delinsAA ENSP00000509861.1:p.Pro547Asn
ENST00000371953.8:c.1120_1121delinsAA MANE Select ENSP00000361021.3:p.Pro374Asn
ENST00000371953.7:c.1120_1121delinsAA ENSP00000361021.3:p.Pro374Asn
NM_000314.5:c.1120_1121delinsAA NP_000305.3:p.Pro374Asn
NM_000314.6:c.1120_1121delinsAA NP_000305.3:p.Pro374Asn
NM_001304717.2:c.1639_1640delinsAA NP_001291646.2:p.Pro547Asn
NM_001304718.1:c.529_530delinsAA NP_001291647.1:p.Pro177Asn
XM_006717926.2:c.1075_1076delinsAA XP_006717989.1:p.Pro359Asn
XM_011539982.1:c.1024_1025delinsAA XP_011538284.1:p.Pro342Asn
XR_945791.1:n.1690_1691delinsAA
NM_000314.7:c.1120_1121delinsAA NP_000305.3:p.Pro374Asn
NM_001304717.5:c.1639_1640delinsAA NP_001291646.4:p.Pro547Asn
NM_001304718.2:c.529_530delinsAA NP_001291647.1:p.Pro177Asn
NM_000314.8:c.1120_1121delinsAA MANE Select NP_000305.3:p.Pro374Asn