Canonical Allele Identifier: CA220637
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 92816
dbSNP Id: rs398123318

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925561_87925564del , CM000672.2:g.87925561_87925564del GRCh38
NC_000010.10:g.89685318_89685321del , CM000672.1:g.89685318_89685321del GRCh37
NC_000010.9:g.89675298_89675301del NCBI36
NG_007466.2:g.67123_67126del , LRG_311:g.67123_67126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.209+4_209+7del ENSP00000514759.2:n.209+4_209+7del
ENST00000710265.1:c.209+4_209+7del ENSP00000518161.1:n.209+4_209+7del
ENST00000472832.3:c.209+4_209+7del ENSP00000483066.2:n.209+4_209+7del
ENST00000688158.2:n.944+4_944+7del
ENST00000688922.2:c.209+4_209+7del ENSP00000508742.2:n.209+4_209+7del
ENST00000700021.1:c.165-5485_165-5482del ENSP00000514757.1:n.165-5485_165-5482del
ENST00000700022.1:c.209+4_209+7del ENSP00000514758.1:n.209+4_209+7del
ENST00000700029.1:c.43+4_43+7del
ENST00000706954.1:c.209+4_209+7del ENSP00000516674.1:n.209+4_209+7del
ENST00000706955.1:c.*244+4_*244+7del ENSP00000516675.1:n.*244+4_*244+7del
ENST00000686459.1:c.209+4_209+7del ENSP00000508909.1:n.209+4_209+7del
ENST00000688158.1:c.*320+4_*320+7del ENSP00000509254.1:n.*320+4_*320+7del
ENST00000688308.1:c.209+4_209+7del ENSP00000508752.1:n.209+4_209+7del
ENST00000688922.1:c.78+4_78+7del
ENST00000693560.1:c.728+4_728+7del ENSP00000509861.1:n.728+4_728+7del
ENST00000371953.8:c.209+4_209+7del MANE Select ENSP00000361021.3:n.209+4_209+7del
ENST00000371953.7:c.209+4_209+7del ENSP00000361021.3:n.209+4_209+7del
ENST00000498703.1:n.35+4_35+7del
ENST00000610634.1:c.107+4_107+7del ENSP00000477517.1:n.107+4_107+7del
NM_000314.5:c.209+4_209+7del NP_000305.3:n.209+4_209+7del
NM_000314.6:c.209+4_209+7del NP_000305.3:n.209+4_209+7del
NM_001304717.2:c.728+4_728+7del NP_001291646.2:n.728+4_728+7del
NM_001304718.1:c.-541-5485_-541-5482del NP_001291647.1:n.-541-5485_-541-5482del
XM_006717926.2:c.165-5485_165-5482del XP_006717989.1:n.165-5485_165-5482del
XM_011539981.1:c.209+4_209+7del XP_011538283.1:n.209+4_209+7del
XM_011539982.1:c.113+4_113+7del XP_011538284.1:n.113+4_113+7del
XR_945789.1:n.921+4_921+7del
XR_945790.1:n.921+4_921+7del
XR_945791.1:n.921+4_921+7del
NM_000314.7:c.209+4_209+7del NP_000305.3:n.209+4_209+7del
NM_001304717.5:c.728+4_728+7del NP_001291646.4:n.728+4_728+7del
NM_001304718.2:c.-541-5485_-541-5482del NP_001291647.1:n.-541-5485_-541-5482del
NM_000314.8:c.209+4_209+7del MANE Select NP_000305.3:n.209+4_209+7del