Canonical Allele Identifier: CA891837870

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933162_87933164delinsGTT , CM000672.2:g.87933162_87933164delinsGTT	GRCh38
NC_000010.10:g.89692919_89692921delinsGTT , CM000672.1:g.89692919_89692921delinsGTT	GRCh37
NC_000010.9:g.89682899_89682901delinsGTT	NCBI36
NG_007466.2:g.74724_74726delinsGTT , LRG_311:g.74724_74726delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.403_405delinsGTT	ENSP00000514759.2:p.Ile135Val
ENST00000710265.1:c.403_405delinsGTT	ENSP00000518161.1:p.Ile135Val
ENST00000472832.3:c.403_405delinsGTT	ENSP00000483066.2:p.Ile135Val
ENST00000688158.2:n.1138_1140delinsGTT
ENST00000688922.2:c.*233_*235delinsGTT	ENSP00000508742.2:n.*233_*235delinsGTT
ENST00000700021.1:c.358_360delinsGTT	ENSP00000514757.1:p.Ile120Val
ENST00000700022.1:c.403_405delinsGTT	ENSP00000514758.1:p.Ile135Val
ENST00000700029.1:c.237_239delinsGTT
ENST00000706954.1:c.403_405delinsGTT	ENSP00000516674.1:p.Ile135Val
ENST00000706955.1:c.*438_*440delinsGTT	ENSP00000516675.1:n.*438_*440delinsGTT
ENST00000686459.1:c.403_405delinsGTT	ENSP00000508909.1:p.Ile135Val
ENST00000688158.1:c.*514_*516delinsGTT	ENSP00000509254.1:n.*514_*516delinsGTT
ENST00000688308.1:c.403_405delinsGTT	ENSP00000508752.1:p.Ile135Val
ENST00000688922.1:c.324_326delinsGTT
ENST00000693560.1:c.922_924delinsGTT	ENSP00000509861.1:p.Ile308Val
ENST00000371953.8:c.403_405delinsGTT MANE Select	ENSP00000361021.3:p.Ile135Val
ENST00000371953.7:c.403_405delinsGTT	ENSP00000361021.3:p.Ile135Val
ENST00000498703.1:n.229_231delinsGTT
ENST00000610634.1:c.301_303delinsGTT	ENSP00000477517.1:p.Ile101Val
NM_000314.5:c.403_405delinsGTT	NP_000305.3:p.Ile135Val
NM_000314.6:c.403_405delinsGTT	NP_000305.3:p.Ile135Val
NM_001304717.2:c.922_924delinsGTT	NP_001291646.2:p.Ile308Val
NM_001304718.1:c.-348_-346delinsGTT	NP_001291647.1:n.-348_-346delinsGTT
XM_006717926.2:c.358_360delinsGTT	XP_006717989.1:p.Ile120Val
XM_011539981.1:c.403_405delinsGTT	XP_011538283.1:p.Ile135Val
XM_011539982.1:c.307_309delinsGTT	XP_011538284.1:p.Ile103Val
XR_945789.1:n.1115_1117delinsGTT
XR_945790.1:n.1115_1117delinsGTT
XR_945791.1:n.1115_1117delinsGTT
NM_000314.7:c.403_405delinsGTT	NP_000305.3:p.Ile135Val
NM_001304717.5:c.922_924delinsGTT	NP_001291646.4:p.Ile308Val
NM_001304718.2:c.-348_-346delinsGTT	NP_001291647.1:n.-348_-346delinsGTT
NM_000314.8:c.403_405delinsGTT MANE Select	NP_000305.3:p.Ile135Val