Canonical Allele Identifier: CA891840834

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933066_87933067delinsTT , CM000672.2:g.87933066_87933067delinsTT	GRCh38
NC_000010.10:g.89692823_89692824delinsTT , CM000672.1:g.89692823_89692824delinsTT	GRCh37
NC_000010.9:g.89682803_89682804delinsTT	NCBI36
NG_007466.2:g.74628_74629delinsTT , LRG_311:g.74628_74629delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.307_308delinsTT	ENSP00000514759.2:p.Pro103Phe
ENST00000710265.1:c.307_308delinsTT	ENSP00000518161.1:p.Pro103Phe
ENST00000472832.3:c.307_308delinsTT	ENSP00000483066.2:p.Pro103Phe
ENST00000688158.2:n.1042_1043delinsTT
ENST00000688922.2:c.*137_*138delinsTT	ENSP00000508742.2:n.*137_*138delinsTT
ENST00000700021.1:c.262_263delinsTT	ENSP00000514757.1:p.Pro88Phe
ENST00000700022.1:c.307_308delinsTT	ENSP00000514758.1:p.Pro103Phe
ENST00000700029.1:c.141_142delinsTT
ENST00000706954.1:c.307_308delinsTT	ENSP00000516674.1:p.Pro103Phe
ENST00000706955.1:c.*342_*343delinsTT	ENSP00000516675.1:n.*342_*343delinsTT
ENST00000686459.1:c.307_308delinsTT	ENSP00000508909.1:p.Pro103Phe
ENST00000688158.1:c.*418_*419delinsTT	ENSP00000509254.1:n.*418_*419delinsTT
ENST00000688308.1:c.307_308delinsTT	ENSP00000508752.1:p.Pro103Phe
ENST00000688922.1:c.228_229delinsTT
ENST00000693560.1:c.826_827delinsTT	ENSP00000509861.1:p.Pro276Phe
ENST00000371953.8:c.307_308delinsTT MANE Select	ENSP00000361021.3:p.Pro103Phe
ENST00000371953.7:c.307_308delinsTT	ENSP00000361021.3:p.Pro103Phe
ENST00000498703.1:n.133_134delinsTT
ENST00000610634.1:c.205_206delinsTT	ENSP00000477517.1:p.Pro69Phe
NM_000314.5:c.307_308delinsTT	NP_000305.3:p.Pro103Phe
NM_000314.6:c.307_308delinsTT	NP_000305.3:p.Pro103Phe
NM_001304717.2:c.826_827delinsTT	NP_001291646.2:p.Pro276Phe
NM_001304718.1:c.-444_-443delinsTT	NP_001291647.1:n.-444_-443delinsTT
XM_006717926.2:c.262_263delinsTT	XP_006717989.1:p.Pro88Phe
XM_011539981.1:c.307_308delinsTT	XP_011538283.1:p.Pro103Phe
XM_011539982.1:c.211_212delinsTT	XP_011538284.1:p.Pro71Phe
XR_945789.1:n.1019_1020delinsTT
XR_945790.1:n.1019_1020delinsTT
XR_945791.1:n.1019_1020delinsTT
NM_000314.7:c.307_308delinsTT	NP_000305.3:p.Pro103Phe
NM_001304717.5:c.826_827delinsTT	NP_001291646.4:p.Pro276Phe
NM_001304718.2:c.-444_-443delinsTT	NP_001291647.1:n.-444_-443delinsTT
NM_000314.8:c.307_308delinsTT MANE Select	NP_000305.3:p.Pro103Phe