Canonical Allele Identifier: CA891838127

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965441_87965442delinsTT , CM000672.2:g.87965441_87965442delinsTT	GRCh38
NC_000010.10:g.89725198_89725199delinsTT , CM000672.1:g.89725198_89725199delinsTT	GRCh37
NC_000010.9:g.89715178_89715179delinsTT	NCBI36
NG_007466.2:g.107003_107004delinsTT , LRG_311:g.107003_107004delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1274_1275delinsTT	ENSP00000514759.2:p.Glu425Val
ENST00000710265.1:c.*210_*211delinsTT	ENSP00000518161.1:n.*210_*211delinsTT
ENST00000688158.2:n.1916_1917delinsTT
ENST00000688922.2:c.*1011_*1012delinsTT	ENSP00000508742.2:n.*1011_*1012delinsTT
ENST00000700021.1:c.1136_1137delinsTT	ENSP00000514757.1:p.Glu379Val
ENST00000700022.1:c.*520_*521delinsTT	ENSP00000514758.1:n.*520_*521delinsTT
ENST00000700023.1:n.2339_2340delinsTT
ENST00000700024.1:n.2573_2574delinsTT
ENST00000706954.1:c.1181_1182delinsTT	ENSP00000516674.1:p.Glu394Val
ENST00000706955.1:c.*1216_*1217delinsTT	ENSP00000516675.1:n.*1216_*1217delinsTT
ENST00000686459.1:c.*767_*768delinsTT	ENSP00000508909.1:n.*767_*768delinsTT
ENST00000688158.1:c.*1292_*1293delinsTT	ENSP00000509254.1:n.*1292_*1293delinsTT
ENST00000688308.1:c.1181_1182delinsTT	ENSP00000508752.1:p.Glu394Val
ENST00000688922.1:c.1102_1103delinsTT
ENST00000693560.1:c.1700_1701delinsTT	ENSP00000509861.1:p.Glu567Val
ENST00000371953.8:c.1181_1182delinsTT MANE Select	ENSP00000361021.3:p.Glu394Val
ENST00000371953.7:c.1181_1182delinsTT	ENSP00000361021.3:p.Glu394Val
NM_000314.5:c.1181_1182delinsTT	NP_000305.3:p.Glu394Val
NM_000314.6:c.1181_1182delinsTT	NP_000305.3:p.Glu394Val
NM_001304717.2:c.1700_1701delinsTT	NP_001291646.2:p.Glu567Val
NM_001304718.1:c.590_591delinsTT	NP_001291647.1:p.Glu197Val
XM_006717926.2:c.1136_1137delinsTT	XP_006717989.1:p.Glu379Val
XM_011539982.1:c.1085_1086delinsTT	XP_011538284.1:p.Glu362Val
XR_945791.1:n.1751_1752delinsTT
NM_000314.7:c.1181_1182delinsTT	NP_000305.3:p.Glu394Val
NM_001304717.5:c.1700_1701delinsTT	NP_001291646.4:p.Glu567Val
NM_001304718.2:c.590_591delinsTT	NP_001291647.1:p.Glu197Val
NM_000314.8:c.1181_1182delinsTT MANE Select	NP_000305.3:p.Glu394Val