Canonical Allele Identifier: CA891841687

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965440_87965442delinsTGT , CM000672.2:g.87965440_87965442delinsTGT	GRCh38
NC_000010.10:g.89725197_89725199delinsTGT , CM000672.1:g.89725197_89725199delinsTGT	GRCh37
NC_000010.9:g.89715177_89715179delinsTGT	NCBI36
NG_007466.2:g.107002_107004delinsTGT , LRG_311:g.107002_107004delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1273_1275delinsTGT	ENSP00000514759.2:p.Glu425Cys
ENST00000710265.1:c.*209_*211delinsTGT	ENSP00000518161.1:n.*209_*211delinsTGT
ENST00000688158.2:n.1915_1917delinsTGT
ENST00000688922.2:c.*1010_*1012delinsTGT	ENSP00000508742.2:n.*1010_*1012delinsTGT
ENST00000700021.1:c.1135_1137delinsTGT	ENSP00000514757.1:p.Glu379Cys
ENST00000700022.1:c.*519_*521delinsTGT	ENSP00000514758.1:n.*519_*521delinsTGT
ENST00000700023.1:n.2338_2340delinsTGT
ENST00000700024.1:n.2572_2574delinsTGT
ENST00000706954.1:c.1180_1182delinsTGT	ENSP00000516674.1:p.Glu394Cys
ENST00000706955.1:c.*1215_*1217delinsTGT	ENSP00000516675.1:n.*1215_*1217delinsTGT
ENST00000686459.1:c.*766_*768delinsTGT	ENSP00000508909.1:n.*766_*768delinsTGT
ENST00000688158.1:c.*1291_*1293delinsTGT	ENSP00000509254.1:n.*1291_*1293delinsTGT
ENST00000688308.1:c.1180_1182delinsTGT	ENSP00000508752.1:p.Glu394Cys
ENST00000688922.1:c.1101_1103delinsTGT
ENST00000693560.1:c.1699_1701delinsTGT	ENSP00000509861.1:p.Glu567Cys
ENST00000371953.8:c.1180_1182delinsTGT MANE Select	ENSP00000361021.3:p.Glu394Cys
ENST00000371953.7:c.1180_1182delinsTGT	ENSP00000361021.3:p.Glu394Cys
NM_000314.5:c.1180_1182delinsTGT	NP_000305.3:p.Glu394Cys
NM_000314.6:c.1180_1182delinsTGT	NP_000305.3:p.Glu394Cys
NM_001304717.2:c.1699_1701delinsTGT	NP_001291646.2:p.Glu567Cys
NM_001304718.1:c.589_591delinsTGT	NP_001291647.1:p.Glu197Cys
XM_006717926.2:c.1135_1137delinsTGT	XP_006717989.1:p.Glu379Cys
XM_011539982.1:c.1084_1086delinsTGT	XP_011538284.1:p.Glu362Cys
XR_945791.1:n.1750_1752delinsTGT
NM_000314.7:c.1180_1182delinsTGT	NP_000305.3:p.Glu394Cys
NM_001304717.5:c.1699_1701delinsTGT	NP_001291646.4:p.Glu567Cys
NM_001304718.2:c.589_591delinsTGT	NP_001291647.1:p.Glu197Cys
NM_000314.8:c.1180_1182delinsTGT MANE Select	NP_000305.3:p.Glu394Cys