Canonical Allele Identifier: CA891836800

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933066_87933068delinsTAT , CM000672.2:g.87933066_87933068delinsTAT	GRCh38
NC_000010.10:g.89692823_89692825delinsTAT , CM000672.1:g.89692823_89692825delinsTAT	GRCh37
NC_000010.9:g.89682803_89682805delinsTAT	NCBI36
NG_007466.2:g.74628_74630delinsTAT , LRG_311:g.74628_74630delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.307_309delinsTAT	ENSP00000514759.2:p.Pro103Tyr
ENST00000710265.1:c.307_309delinsTAT	ENSP00000518161.1:p.Pro103Tyr
ENST00000472832.3:c.307_309delinsTAT	ENSP00000483066.2:p.Pro103Tyr
ENST00000688158.2:n.1042_1044delinsTAT
ENST00000688922.2:c.*137_*139delinsTAT	ENSP00000508742.2:n.*137_*139delinsTAT
ENST00000700021.1:c.262_264delinsTAT	ENSP00000514757.1:p.Pro88Tyr
ENST00000700022.1:c.307_309delinsTAT	ENSP00000514758.1:p.Pro103Tyr
ENST00000700029.1:c.141_143delinsTAT
ENST00000706954.1:c.307_309delinsTAT	ENSP00000516674.1:p.Pro103Tyr
ENST00000706955.1:c.*342_*344delinsTAT	ENSP00000516675.1:n.*342_*344delinsTAT
ENST00000686459.1:c.307_309delinsTAT	ENSP00000508909.1:p.Pro103Tyr
ENST00000688158.1:c.*418_*420delinsTAT	ENSP00000509254.1:n.*418_*420delinsTAT
ENST00000688308.1:c.307_309delinsTAT	ENSP00000508752.1:p.Pro103Tyr
ENST00000688922.1:c.228_230delinsTAT
ENST00000693560.1:c.826_828delinsTAT	ENSP00000509861.1:p.Pro276Tyr
ENST00000371953.8:c.307_309delinsTAT MANE Select	ENSP00000361021.3:p.Pro103Tyr
ENST00000371953.7:c.307_309delinsTAT	ENSP00000361021.3:p.Pro103Tyr
ENST00000498703.1:n.133_135delinsTAT
ENST00000610634.1:c.205_207delinsTAT	ENSP00000477517.1:p.Pro69Tyr
NM_000314.5:c.307_309delinsTAT	NP_000305.3:p.Pro103Tyr
NM_000314.6:c.307_309delinsTAT	NP_000305.3:p.Pro103Tyr
NM_001304717.2:c.826_828delinsTAT	NP_001291646.2:p.Pro276Tyr
NM_001304718.1:c.-444_-442delinsTAT	NP_001291647.1:n.-444_-442delinsTAT
XM_006717926.2:c.262_264delinsTAT	XP_006717989.1:p.Pro88Tyr
XM_011539981.1:c.307_309delinsTAT	XP_011538283.1:p.Pro103Tyr
XM_011539982.1:c.211_213delinsTAT	XP_011538284.1:p.Pro71Tyr
XR_945789.1:n.1019_1021delinsTAT
XR_945790.1:n.1019_1021delinsTAT
XR_945791.1:n.1019_1021delinsTAT
NM_000314.7:c.307_309delinsTAT	NP_000305.3:p.Pro103Tyr
NM_001304717.5:c.826_828delinsTAT	NP_001291646.4:p.Pro276Tyr
NM_001304718.2:c.-444_-442delinsTAT	NP_001291647.1:n.-444_-442delinsTAT
NM_000314.8:c.307_309delinsTAT MANE Select	NP_000305.3:p.Pro103Tyr