Canonical Allele Identifier: CA891838117

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965440_87965442delinsTAT , CM000672.2:g.87965440_87965442delinsTAT	GRCh38
NC_000010.10:g.89725197_89725199delinsTAT , CM000672.1:g.89725197_89725199delinsTAT	GRCh37
NC_000010.9:g.89715177_89715179delinsTAT	NCBI36
NG_007466.2:g.107002_107004delinsTAT , LRG_311:g.107002_107004delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1273_1275delinsTAT	ENSP00000514759.2:p.Glu425Tyr
ENST00000710265.1:c.*209_*211delinsTAT	ENSP00000518161.1:n.*209_*211delinsTAT
ENST00000688158.2:n.1915_1917delinsTAT
ENST00000688922.2:c.*1010_*1012delinsTAT	ENSP00000508742.2:n.*1010_*1012delinsTAT
ENST00000700021.1:c.1135_1137delinsTAT	ENSP00000514757.1:p.Glu379Tyr
ENST00000700022.1:c.*519_*521delinsTAT	ENSP00000514758.1:n.*519_*521delinsTAT
ENST00000700023.1:n.2338_2340delinsTAT
ENST00000700024.1:n.2572_2574delinsTAT
ENST00000706954.1:c.1180_1182delinsTAT	ENSP00000516674.1:p.Glu394Tyr
ENST00000706955.1:c.*1215_*1217delinsTAT	ENSP00000516675.1:n.*1215_*1217delinsTAT
ENST00000686459.1:c.*766_*768delinsTAT	ENSP00000508909.1:n.*766_*768delinsTAT
ENST00000688158.1:c.*1291_*1293delinsTAT	ENSP00000509254.1:n.*1291_*1293delinsTAT
ENST00000688308.1:c.1180_1182delinsTAT	ENSP00000508752.1:p.Glu394Tyr
ENST00000688922.1:c.1101_1103delinsTAT
ENST00000693560.1:c.1699_1701delinsTAT	ENSP00000509861.1:p.Glu567Tyr
ENST00000371953.8:c.1180_1182delinsTAT MANE Select	ENSP00000361021.3:p.Glu394Tyr
ENST00000371953.7:c.1180_1182delinsTAT	ENSP00000361021.3:p.Glu394Tyr
NM_000314.5:c.1180_1182delinsTAT	NP_000305.3:p.Glu394Tyr
NM_000314.6:c.1180_1182delinsTAT	NP_000305.3:p.Glu394Tyr
NM_001304717.2:c.1699_1701delinsTAT	NP_001291646.2:p.Glu567Tyr
NM_001304718.1:c.589_591delinsTAT	NP_001291647.1:p.Glu197Tyr
XM_006717926.2:c.1135_1137delinsTAT	XP_006717989.1:p.Glu379Tyr
XM_011539982.1:c.1084_1086delinsTAT	XP_011538284.1:p.Glu362Tyr
XR_945791.1:n.1750_1752delinsTAT
NM_000314.7:c.1180_1182delinsTAT	NP_000305.3:p.Glu394Tyr
NM_001304717.5:c.1699_1701delinsTAT	NP_001291646.4:p.Glu567Tyr
NM_001304718.2:c.589_591delinsTAT	NP_001291647.1:p.Glu197Tyr
NM_000314.8:c.1180_1182delinsTAT MANE Select	NP_000305.3:p.Glu394Tyr