Canonical Allele Identifier: CA891837604
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965371_87965373delinsTTG , CM000672.2:g.87965371_87965373delinsTTG GRCh38
NC_000010.10:g.89725128_89725130delinsTTG , CM000672.1:g.89725128_89725130delinsTTG GRCh37
NC_000010.9:g.89715108_89715110delinsTTG NCBI36
NG_007466.2:g.106933_106935delinsTTG , LRG_311:g.106933_106935delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1204_1206delinsTTG ENSP00000514759.2:p.Asp402Leu
ENST00000710265.1:c.*140_*142delinsTTG ENSP00000518161.1:n.*140_*142delinsTTG
ENST00000688158.2:n.1846_1848delinsTTG
ENST00000688922.2:c.*941_*943delinsTTG ENSP00000508742.2:n.*941_*943delinsTTG
ENST00000700021.1:c.1066_1068delinsTTG ENSP00000514757.1:p.Asp356Leu
ENST00000700022.1:c.*450_*452delinsTTG ENSP00000514758.1:n.*450_*452delinsTTG
ENST00000700023.1:n.2269_2271delinsTTG
ENST00000700024.1:n.2503_2505delinsTTG
ENST00000706954.1:c.1111_1113delinsTTG ENSP00000516674.1:p.Asp371Leu
ENST00000706955.1:c.*1146_*1148delinsTTG ENSP00000516675.1:n.*1146_*1148delinsTTG
ENST00000686459.1:c.*697_*699delinsTTG ENSP00000508909.1:n.*697_*699delinsTTG
ENST00000688158.1:c.*1222_*1224delinsTTG ENSP00000509254.1:n.*1222_*1224delinsTTG
ENST00000688308.1:c.1111_1113delinsTTG ENSP00000508752.1:p.Asp371Leu
ENST00000688922.1:c.1032_1034delinsTTG
ENST00000693560.1:c.1630_1632delinsTTG ENSP00000509861.1:p.Asp544Leu
ENST00000371953.8:c.1111_1113delinsTTG MANE Select ENSP00000361021.3:p.Asp371Leu
ENST00000371953.7:c.1111_1113delinsTTG ENSP00000361021.3:p.Asp371Leu
NM_000314.5:c.1111_1113delinsTTG NP_000305.3:p.Asp371Leu
NM_000314.6:c.1111_1113delinsTTG NP_000305.3:p.Asp371Leu
NM_001304717.2:c.1630_1632delinsTTG NP_001291646.2:p.Asp544Leu
NM_001304718.1:c.520_522delinsTTG NP_001291647.1:p.Asp174Leu
XM_006717926.2:c.1066_1068delinsTTG XP_006717989.1:p.Asp356Leu
XM_011539982.1:c.1015_1017delinsTTG XP_011538284.1:p.Asp339Leu
XR_945791.1:n.1681_1683delinsTTG
NM_000314.7:c.1111_1113delinsTTG NP_000305.3:p.Asp371Leu
NM_001304717.5:c.1630_1632delinsTTG NP_001291646.4:p.Asp544Leu
NM_001304718.2:c.520_522delinsTTG NP_001291647.1:p.Asp174Leu
NM_000314.8:c.1111_1113delinsTTG MANE Select NP_000305.3:p.Asp371Leu