Canonical Allele Identifier: CA891841686

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965440_87965442delinsTTT , CM000672.2:g.87965440_87965442delinsTTT	GRCh38
NC_000010.10:g.89725197_89725199delinsTTT , CM000672.1:g.89725197_89725199delinsTTT	GRCh37
NC_000010.9:g.89715177_89715179delinsTTT	NCBI36
NG_007466.2:g.107002_107004delinsTTT , LRG_311:g.107002_107004delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1273_1275delinsTTT	ENSP00000514759.2:p.Glu425Phe
ENST00000710265.1:c.*209_*211delinsTTT	ENSP00000518161.1:n.*209_*211delinsTTT
ENST00000688158.2:n.1915_1917delinsTTT
ENST00000688922.2:c.*1010_*1012delinsTTT	ENSP00000508742.2:n.*1010_*1012delinsTTT
ENST00000700021.1:c.1135_1137delinsTTT	ENSP00000514757.1:p.Glu379Phe
ENST00000700022.1:c.*519_*521delinsTTT	ENSP00000514758.1:n.*519_*521delinsTTT
ENST00000700023.1:n.2338_2340delinsTTT
ENST00000700024.1:n.2572_2574delinsTTT
ENST00000706954.1:c.1180_1182delinsTTT	ENSP00000516674.1:p.Glu394Phe
ENST00000706955.1:c.*1215_*1217delinsTTT	ENSP00000516675.1:n.*1215_*1217delinsTTT
ENST00000686459.1:c.*766_*768delinsTTT	ENSP00000508909.1:n.*766_*768delinsTTT
ENST00000688158.1:c.*1291_*1293delinsTTT	ENSP00000509254.1:n.*1291_*1293delinsTTT
ENST00000688308.1:c.1180_1182delinsTTT	ENSP00000508752.1:p.Glu394Phe
ENST00000688922.1:c.1101_1103delinsTTT
ENST00000693560.1:c.1699_1701delinsTTT	ENSP00000509861.1:p.Glu567Phe
ENST00000371953.8:c.1180_1182delinsTTT MANE Select	ENSP00000361021.3:p.Glu394Phe
ENST00000371953.7:c.1180_1182delinsTTT	ENSP00000361021.3:p.Glu394Phe
NM_000314.5:c.1180_1182delinsTTT	NP_000305.3:p.Glu394Phe
NM_000314.6:c.1180_1182delinsTTT	NP_000305.3:p.Glu394Phe
NM_001304717.2:c.1699_1701delinsTTT	NP_001291646.2:p.Glu567Phe
NM_001304718.1:c.589_591delinsTTT	NP_001291647.1:p.Glu197Phe
XM_006717926.2:c.1135_1137delinsTTT	XP_006717989.1:p.Glu379Phe
XM_011539982.1:c.1084_1086delinsTTT	XP_011538284.1:p.Glu362Phe
XR_945791.1:n.1750_1752delinsTTT
NM_000314.7:c.1180_1182delinsTTT	NP_000305.3:p.Glu394Phe
NM_001304717.5:c.1699_1701delinsTTT	NP_001291646.4:p.Glu567Phe
NM_001304718.2:c.589_591delinsTTT	NP_001291647.1:p.Glu197Phe
NM_000314.8:c.1180_1182delinsTTT MANE Select	NP_000305.3:p.Glu394Phe