Canonical Allele Identifier: CA891837591
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965371_87965373delinsTAA , CM000672.2:g.87965371_87965373delinsTAA GRCh38
NC_000010.10:g.89725128_89725130delinsTAA , CM000672.1:g.89725128_89725130delinsTAA GRCh37
NC_000010.9:g.89715108_89715110delinsTAA NCBI36
NG_007466.2:g.106933_106935delinsTAA , LRG_311:g.106933_106935delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1204_1206delinsTAA ENSP00000514759.2:p.Asp402Ter
ENST00000710265.1:c.*140_*142delinsTAA ENSP00000518161.1:n.*140_*142delinsTAA
ENST00000688158.2:n.1846_1848delinsTAA
ENST00000688922.2:c.*941_*943delinsTAA ENSP00000508742.2:n.*941_*943delinsTAA
ENST00000700021.1:c.1066_1068delinsTAA ENSP00000514757.1:p.Asp356Ter
ENST00000700022.1:c.*450_*452delinsTAA ENSP00000514758.1:n.*450_*452delinsTAA
ENST00000700023.1:n.2269_2271delinsTAA
ENST00000700024.1:n.2503_2505delinsTAA
ENST00000706954.1:c.1111_1113delinsTAA ENSP00000516674.1:p.Asp371Ter
ENST00000706955.1:c.*1146_*1148delinsTAA ENSP00000516675.1:n.*1146_*1148delinsTAA
ENST00000686459.1:c.*697_*699delinsTAA ENSP00000508909.1:n.*697_*699delinsTAA
ENST00000688158.1:c.*1222_*1224delinsTAA ENSP00000509254.1:n.*1222_*1224delinsTAA
ENST00000688308.1:c.1111_1113delinsTAA ENSP00000508752.1:p.Asp371Ter
ENST00000688922.1:c.1032_1034delinsTAA
ENST00000693560.1:c.1630_1632delinsTAA ENSP00000509861.1:p.Asp544Ter
ENST00000371953.8:c.1111_1113delinsTAA MANE Select ENSP00000361021.3:p.Asp371Ter
ENST00000371953.7:c.1111_1113delinsTAA ENSP00000361021.3:p.Asp371Ter
NM_000314.5:c.1111_1113delinsTAA NP_000305.3:p.Asp371Ter
NM_000314.6:c.1111_1113delinsTAA NP_000305.3:p.Asp371Ter
NM_001304717.2:c.1630_1632delinsTAA NP_001291646.2:p.Asp544Ter
NM_001304718.1:c.520_522delinsTAA NP_001291647.1:p.Asp174Ter
XM_006717926.2:c.1066_1068delinsTAA XP_006717989.1:p.Asp356Ter
XM_011539982.1:c.1015_1017delinsTAA XP_011538284.1:p.Asp339Ter
XR_945791.1:n.1681_1683delinsTAA
NM_000314.7:c.1111_1113delinsTAA NP_000305.3:p.Asp371Ter
NM_001304717.5:c.1630_1632delinsTAA NP_001291646.4:p.Asp544Ter
NM_001304718.2:c.520_522delinsTAA NP_001291647.1:p.Asp174Ter
NM_000314.8:c.1111_1113delinsTAA MANE Select NP_000305.3:p.Asp371Ter