Canonical Allele Identifier: CA891837603
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965371_87965373delinsATG , CM000672.2:g.87965371_87965373delinsATG GRCh38
NC_000010.10:g.89725128_89725130delinsATG , CM000672.1:g.89725128_89725130delinsATG GRCh37
NC_000010.9:g.89715108_89715110delinsATG NCBI36
NG_007466.2:g.106933_106935delinsATG , LRG_311:g.106933_106935delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1204_1206delinsATG ENSP00000514759.2:p.Asp402Met
ENST00000710265.1:c.*140_*142delinsATG ENSP00000518161.1:n.*140_*142delinsATG
ENST00000688158.2:n.1846_1848delinsATG
ENST00000688922.2:c.*941_*943delinsATG ENSP00000508742.2:n.*941_*943delinsATG
ENST00000700021.1:c.1066_1068delinsATG ENSP00000514757.1:p.Asp356Met
ENST00000700022.1:c.*450_*452delinsATG ENSP00000514758.1:n.*450_*452delinsATG
ENST00000700023.1:n.2269_2271delinsATG
ENST00000700024.1:n.2503_2505delinsATG
ENST00000706954.1:c.1111_1113delinsATG ENSP00000516674.1:p.Asp371Met
ENST00000706955.1:c.*1146_*1148delinsATG ENSP00000516675.1:n.*1146_*1148delinsATG
ENST00000686459.1:c.*697_*699delinsATG ENSP00000508909.1:n.*697_*699delinsATG
ENST00000688158.1:c.*1222_*1224delinsATG ENSP00000509254.1:n.*1222_*1224delinsATG
ENST00000688308.1:c.1111_1113delinsATG ENSP00000508752.1:p.Asp371Met
ENST00000688922.1:c.1032_1034delinsATG
ENST00000693560.1:c.1630_1632delinsATG ENSP00000509861.1:p.Asp544Met
ENST00000371953.8:c.1111_1113delinsATG MANE Select ENSP00000361021.3:p.Asp371Met
ENST00000371953.7:c.1111_1113delinsATG ENSP00000361021.3:p.Asp371Met
NM_000314.5:c.1111_1113delinsATG NP_000305.3:p.Asp371Met
NM_000314.6:c.1111_1113delinsATG NP_000305.3:p.Asp371Met
NM_001304717.2:c.1630_1632delinsATG NP_001291646.2:p.Asp544Met
NM_001304718.1:c.520_522delinsATG NP_001291647.1:p.Asp174Met
XM_006717926.2:c.1066_1068delinsATG XP_006717989.1:p.Asp356Met
XM_011539982.1:c.1015_1017delinsATG XP_011538284.1:p.Asp339Met
XR_945791.1:n.1681_1683delinsATG
NM_000314.7:c.1111_1113delinsATG NP_000305.3:p.Asp371Met
NM_001304717.5:c.1630_1632delinsATG NP_001291646.4:p.Asp544Met
NM_001304718.2:c.520_522delinsATG NP_001291647.1:p.Asp174Met
NM_000314.8:c.1111_1113delinsATG MANE Select NP_000305.3:p.Asp371Met