Canonical Allele Identifier: CA891836601

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933048_87933050delinsGCT , CM000672.2:g.87933048_87933050delinsGCT	GRCh38
NC_000010.10:g.89692805_89692807delinsGCT , CM000672.1:g.89692805_89692807delinsGCT	GRCh37
NC_000010.9:g.89682785_89682787delinsGCT	NCBI36
NG_007466.2:g.74610_74612delinsGCT , LRG_311:g.74610_74612delinsGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.289_291delinsGCT	ENSP00000514759.2:p.Gln97Ala
ENST00000710265.1:c.289_291delinsGCT	ENSP00000518161.1:p.Gln97Ala
ENST00000472832.3:c.289_291delinsGCT	ENSP00000483066.2:p.Gln97Ala
ENST00000688158.2:n.1024_1026delinsGCT
ENST00000688922.2:c.*119_*121delinsGCT	ENSP00000508742.2:n.*119_*121delinsGCT
ENST00000700021.1:c.244_246delinsGCT	ENSP00000514757.1:p.Gln82Ala
ENST00000700022.1:c.289_291delinsGCT	ENSP00000514758.1:p.Gln97Ala
ENST00000700029.1:c.123_125delinsGCT
ENST00000706954.1:c.289_291delinsGCT	ENSP00000516674.1:p.Gln97Ala
ENST00000706955.1:c.*324_*326delinsGCT	ENSP00000516675.1:n.*324_*326delinsGCT
ENST00000686459.1:c.289_291delinsGCT	ENSP00000508909.1:p.Gln97Ala
ENST00000688158.1:c.*400_*402delinsGCT	ENSP00000509254.1:n.*400_*402delinsGCT
ENST00000688308.1:c.289_291delinsGCT	ENSP00000508752.1:p.Gln97Ala
ENST00000688922.1:c.210_212delinsGCT
ENST00000693560.1:c.808_810delinsGCT	ENSP00000509861.1:p.Gln270Ala
ENST00000371953.8:c.289_291delinsGCT MANE Select	ENSP00000361021.3:p.Gln97Ala
ENST00000371953.7:c.289_291delinsGCT	ENSP00000361021.3:p.Gln97Ala
ENST00000498703.1:n.115_117delinsGCT
ENST00000610634.1:c.187_189delinsGCT	ENSP00000477517.1:p.Gln63Ala
NM_000314.5:c.289_291delinsGCT	NP_000305.3:p.Gln97Ala
NM_000314.6:c.289_291delinsGCT	NP_000305.3:p.Gln97Ala
NM_001304717.2:c.808_810delinsGCT	NP_001291646.2:p.Gln270Ala
NM_001304718.1:c.-462_-460delinsGCT	NP_001291647.1:n.-462_-460delinsGCT
XM_006717926.2:c.244_246delinsGCT	XP_006717989.1:p.Gln82Ala
XM_011539981.1:c.289_291delinsGCT	XP_011538283.1:p.Gln97Ala
XM_011539982.1:c.193_195delinsGCT	XP_011538284.1:p.Gln65Ala
XR_945789.1:n.1001_1003delinsGCT
XR_945790.1:n.1001_1003delinsGCT
XR_945791.1:n.1001_1003delinsGCT
NM_000314.7:c.289_291delinsGCT	NP_000305.3:p.Gln97Ala
NM_001304717.5:c.808_810delinsGCT	NP_001291646.4:p.Gln270Ala
NM_001304718.2:c.-462_-460delinsGCT	NP_001291647.1:n.-462_-460delinsGCT
NM_000314.8:c.289_291delinsGCT MANE Select	NP_000305.3:p.Gln97Ala