Canonical Allele Identifier: CA891836602

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933048_87933050delinsATT , CM000672.2:g.87933048_87933050delinsATT	GRCh38
NC_000010.10:g.89692805_89692807delinsATT , CM000672.1:g.89692805_89692807delinsATT	GRCh37
NC_000010.9:g.89682785_89682787delinsATT	NCBI36
NG_007466.2:g.74610_74612delinsATT , LRG_311:g.74610_74612delinsATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.289_291delinsATT	ENSP00000514759.2:p.Gln97Ile
ENST00000710265.1:c.289_291delinsATT	ENSP00000518161.1:p.Gln97Ile
ENST00000472832.3:c.289_291delinsATT	ENSP00000483066.2:p.Gln97Ile
ENST00000688158.2:n.1024_1026delinsATT
ENST00000688922.2:c.*119_*121delinsATT	ENSP00000508742.2:n.*119_*121delinsATT
ENST00000700021.1:c.244_246delinsATT	ENSP00000514757.1:p.Gln82Ile
ENST00000700022.1:c.289_291delinsATT	ENSP00000514758.1:p.Gln97Ile
ENST00000700029.1:c.123_125delinsATT
ENST00000706954.1:c.289_291delinsATT	ENSP00000516674.1:p.Gln97Ile
ENST00000706955.1:c.*324_*326delinsATT	ENSP00000516675.1:n.*324_*326delinsATT
ENST00000686459.1:c.289_291delinsATT	ENSP00000508909.1:p.Gln97Ile
ENST00000688158.1:c.*400_*402delinsATT	ENSP00000509254.1:n.*400_*402delinsATT
ENST00000688308.1:c.289_291delinsATT	ENSP00000508752.1:p.Gln97Ile
ENST00000688922.1:c.210_212delinsATT
ENST00000693560.1:c.808_810delinsATT	ENSP00000509861.1:p.Gln270Ile
ENST00000371953.8:c.289_291delinsATT MANE Select	ENSP00000361021.3:p.Gln97Ile
ENST00000371953.7:c.289_291delinsATT	ENSP00000361021.3:p.Gln97Ile
ENST00000498703.1:n.115_117delinsATT
ENST00000610634.1:c.187_189delinsATT	ENSP00000477517.1:p.Gln63Ile
NM_000314.5:c.289_291delinsATT	NP_000305.3:p.Gln97Ile
NM_000314.6:c.289_291delinsATT	NP_000305.3:p.Gln97Ile
NM_001304717.2:c.808_810delinsATT	NP_001291646.2:p.Gln270Ile
NM_001304718.1:c.-462_-460delinsATT	NP_001291647.1:n.-462_-460delinsATT
XM_006717926.2:c.244_246delinsATT	XP_006717989.1:p.Gln82Ile
XM_011539981.1:c.289_291delinsATT	XP_011538283.1:p.Gln97Ile
XM_011539982.1:c.193_195delinsATT	XP_011538284.1:p.Gln65Ile
XR_945789.1:n.1001_1003delinsATT
XR_945790.1:n.1001_1003delinsATT
XR_945791.1:n.1001_1003delinsATT
NM_000314.7:c.289_291delinsATT	NP_000305.3:p.Gln97Ile
NM_001304717.5:c.808_810delinsATT	NP_001291646.4:p.Gln270Ile
NM_001304718.2:c.-462_-460delinsATT	NP_001291647.1:n.-462_-460delinsATT
NM_000314.8:c.289_291delinsATT MANE Select	NP_000305.3:p.Gln97Ile