Canonical Allele Identifier: CA891837864

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933162_87933163delinsCA , CM000672.2:g.87933162_87933163delinsCA	GRCh38
NC_000010.10:g.89692919_89692920delinsCA , CM000672.1:g.89692919_89692920delinsCA	GRCh37
NC_000010.9:g.89682899_89682900delinsCA	NCBI36
NG_007466.2:g.74724_74725delinsCA , LRG_311:g.74724_74725delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.403_404delinsCA	ENSP00000514759.2:p.Ile135Gln
ENST00000710265.1:c.403_404delinsCA	ENSP00000518161.1:p.Ile135Gln
ENST00000472832.3:c.403_404delinsCA	ENSP00000483066.2:p.Ile135Gln
ENST00000688158.2:n.1138_1139delinsCA
ENST00000688922.2:c.*233_*234delinsCA	ENSP00000508742.2:n.*233_*234delinsCA
ENST00000700021.1:c.358_359delinsCA	ENSP00000514757.1:p.Ile120Gln
ENST00000700022.1:c.403_404delinsCA	ENSP00000514758.1:p.Ile135Gln
ENST00000700029.1:c.237_238delinsCA
ENST00000706954.1:c.403_404delinsCA	ENSP00000516674.1:p.Ile135Gln
ENST00000706955.1:c.*438_*439delinsCA	ENSP00000516675.1:n.*438_*439delinsCA
ENST00000686459.1:c.403_404delinsCA	ENSP00000508909.1:p.Ile135Gln
ENST00000688158.1:c.*514_*515delinsCA	ENSP00000509254.1:n.*514_*515delinsCA
ENST00000688308.1:c.403_404delinsCA	ENSP00000508752.1:p.Ile135Gln
ENST00000688922.1:c.324_325delinsCA
ENST00000693560.1:c.922_923delinsCA	ENSP00000509861.1:p.Ile308Gln
ENST00000371953.8:c.403_404delinsCA MANE Select	ENSP00000361021.3:p.Ile135Gln
ENST00000371953.7:c.403_404delinsCA	ENSP00000361021.3:p.Ile135Gln
ENST00000498703.1:n.229_230delinsCA
ENST00000610634.1:c.301_302delinsCA	ENSP00000477517.1:p.Ile101Gln
NM_000314.5:c.403_404delinsCA	NP_000305.3:p.Ile135Gln
NM_000314.6:c.403_404delinsCA	NP_000305.3:p.Ile135Gln
NM_001304717.2:c.922_923delinsCA	NP_001291646.2:p.Ile308Gln
NM_001304718.1:c.-348_-347delinsCA	NP_001291647.1:n.-348_-347delinsCA
XM_006717926.2:c.358_359delinsCA	XP_006717989.1:p.Ile120Gln
XM_011539981.1:c.403_404delinsCA	XP_011538283.1:p.Ile135Gln
XM_011539982.1:c.307_308delinsCA	XP_011538284.1:p.Ile103Gln
XR_945789.1:n.1115_1116delinsCA
XR_945790.1:n.1115_1116delinsCA
XR_945791.1:n.1115_1116delinsCA
NM_000314.7:c.403_404delinsCA	NP_000305.3:p.Ile135Gln
NM_001304717.5:c.922_923delinsCA	NP_001291646.4:p.Ile308Gln
NM_001304718.2:c.-348_-347delinsCA	NP_001291647.1:n.-348_-347delinsCA
NM_000314.8:c.403_404delinsCA MANE Select	NP_000305.3:p.Ile135Gln