Canonical Allele Identifier: CA2579986001
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965443_87965445delinsCCA , CM000672.2:g.87965443_87965445delinsCCA GRCh38
NC_000010.10:g.89725200_89725202delinsCCA , CM000672.1:g.89725200_89725202delinsCCA GRCh37
NC_000010.9:g.89715180_89715182delinsCCA NCBI36
NG_007466.2:g.107005_107007delinsCCA , LRG_311:g.107005_107007delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1276_1278delinsCCA ENSP00000514759.2:p.Asp426Pro
ENST00000710265.1:c.*212_*214delinsCCA ENSP00000518161.1:n.*212_*214delinsCCA
ENST00000688158.2:n.1918_1920delinsCCA
ENST00000688922.2:c.*1013_*1015delinsCCA ENSP00000508742.2:n.*1013_*1015delinsCCA
ENST00000700021.1:c.1138_1140delinsCCA ENSP00000514757.1:p.Asp380Pro
ENST00000700022.1:c.*522_*524delinsCCA ENSP00000514758.1:n.*522_*524delinsCCA
ENST00000700023.1:n.2341_2343delinsCCA
ENST00000700024.1:n.2575_2577delinsCCA
ENST00000706954.1:c.1183_1185delinsCCA ENSP00000516674.1:p.Asp395Pro
ENST00000706955.1:c.*1218_*1220delinsCCA ENSP00000516675.1:n.*1218_*1220delinsCCA
ENST00000686459.1:c.*769_*771delinsCCA ENSP00000508909.1:n.*769_*771delinsCCA
ENST00000688158.1:c.*1294_*1296delinsCCA ENSP00000509254.1:n.*1294_*1296delinsCCA
ENST00000688308.1:c.1183_1185delinsCCA ENSP00000508752.1:p.Asp395Pro
ENST00000688922.1:c.1104_1106delinsCCA
ENST00000693560.1:c.1702_1704delinsCCA ENSP00000509861.1:p.Asp568Pro
ENST00000371953.8:c.1183_1185delinsCCA MANE Select ENSP00000361021.3:p.Asp395Pro
ENST00000371953.7:c.1183_1185delinsCCA ENSP00000361021.3:p.Asp395Pro
NM_000314.5:c.1183_1185delinsCCA NP_000305.3:p.Asp395Pro
NM_000314.6:c.1183_1185delinsCCA NP_000305.3:p.Asp395Pro
NM_001304717.2:c.1702_1704delinsCCA NP_001291646.2:p.Asp568Pro
NM_001304718.1:c.592_594delinsCCA NP_001291647.1:p.Asp198Pro
XM_006717926.2:c.1138_1140delinsCCA XP_006717989.1:p.Asp380Pro
XM_011539982.1:c.1087_1089delinsCCA XP_011538284.1:p.Asp363Pro
XR_945791.1:n.1753_1755delinsCCA
NM_000314.7:c.1183_1185delinsCCA NP_000305.3:p.Asp395Pro
NM_001304717.5:c.1702_1704delinsCCA NP_001291646.4:p.Asp568Pro
NM_001304718.2:c.592_594delinsCCA NP_001291647.1:p.Asp198Pro
NM_000314.8:c.1183_1185delinsCCA MANE Select NP_000305.3:p.Asp395Pro