Canonical Allele Identifier: CA2579986002
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965443_87965444delinsTT , CM000672.2:g.87965443_87965444delinsTT GRCh38
NC_000010.10:g.89725200_89725201delinsTT , CM000672.1:g.89725200_89725201delinsTT GRCh37
NC_000010.9:g.89715180_89715181delinsTT NCBI36
NG_007466.2:g.107005_107006delinsTT , LRG_311:g.107005_107006delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1276_1277delinsTT ENSP00000514759.2:p.Asp426Phe
ENST00000710265.1:c.*212_*213delinsTT ENSP00000518161.1:n.*212_*213delinsTT
ENST00000688158.2:n.1918_1919delinsTT
ENST00000688922.2:c.*1013_*1014delinsTT ENSP00000508742.2:n.*1013_*1014delinsTT
ENST00000700021.1:c.1138_1139delinsTT ENSP00000514757.1:p.Asp380Phe
ENST00000700022.1:c.*522_*523delinsTT ENSP00000514758.1:n.*522_*523delinsTT
ENST00000700023.1:n.2341_2342delinsTT
ENST00000700024.1:n.2575_2576delinsTT
ENST00000706954.1:c.1183_1184delinsTT ENSP00000516674.1:p.Asp395Phe
ENST00000706955.1:c.*1218_*1219delinsTT ENSP00000516675.1:n.*1218_*1219delinsTT
ENST00000686459.1:c.*769_*770delinsTT ENSP00000508909.1:n.*769_*770delinsTT
ENST00000688158.1:c.*1294_*1295delinsTT ENSP00000509254.1:n.*1294_*1295delinsTT
ENST00000688308.1:c.1183_1184delinsTT ENSP00000508752.1:p.Asp395Phe
ENST00000688922.1:c.1104_1105delinsTT
ENST00000693560.1:c.1702_1703delinsTT ENSP00000509861.1:p.Asp568Phe
ENST00000371953.8:c.1183_1184delinsTT MANE Select ENSP00000361021.3:p.Asp395Phe
ENST00000371953.7:c.1183_1184delinsTT ENSP00000361021.3:p.Asp395Phe
NM_000314.5:c.1183_1184delinsTT NP_000305.3:p.Asp395Phe
NM_000314.6:c.1183_1184delinsTT NP_000305.3:p.Asp395Phe
NM_001304717.2:c.1702_1703delinsTT NP_001291646.2:p.Asp568Phe
NM_001304718.1:c.592_593delinsTT NP_001291647.1:p.Asp198Phe
XM_006717926.2:c.1138_1139delinsTT XP_006717989.1:p.Asp380Phe
XM_011539982.1:c.1087_1088delinsTT XP_011538284.1:p.Asp363Phe
XR_945791.1:n.1753_1754delinsTT
NM_000314.7:c.1183_1184delinsTT NP_000305.3:p.Asp395Phe
NM_001304717.5:c.1702_1703delinsTT NP_001291646.4:p.Asp568Phe
NM_001304718.2:c.592_593delinsTT NP_001291647.1:p.Asp198Phe
NM_000314.8:c.1183_1184delinsTT MANE Select NP_000305.3:p.Asp395Phe