Canonical Allele Identifier: CA891835246

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960963_87960965delinsACT , CM000672.2:g.87960963_87960965delinsACT	GRCh38
NC_000010.10:g.89720720_89720722delinsACT , CM000672.1:g.89720720_89720722delinsACT	GRCh37
NC_000010.9:g.89710700_89710702delinsACT	NCBI36
NG_007466.2:g.102525_102527delinsACT , LRG_311:g.102525_102527delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.964_966delinsACT	ENSP00000514759.2:p.Glu322Thr
ENST00000710265.1:c.871_873delinsACT	ENSP00000518161.1:p.Glu291Thr
ENST00000472832.3:c.871_873delinsACT	ENSP00000483066.2:p.Glu291Thr
ENST00000688158.2:n.1606_1608delinsACT
ENST00000688922.2:c.*701_*703delinsACT	ENSP00000508742.2:n.*701_*703delinsACT
ENST00000700021.1:c.826_828delinsACT	ENSP00000514757.1:p.Glu276Thr
ENST00000700022.1:c.*210_*212delinsACT	ENSP00000514758.1:n.*210_*212delinsACT
ENST00000700023.1:n.2029_2031delinsACT
ENST00000700024.1:n.2263_2265delinsACT
ENST00000700025.1:n.1640_1642delinsACT
ENST00000700026.1:n.508_510delinsACT
ENST00000700029.1:c.798_800delinsACT
ENST00000706954.1:c.871_873delinsACT	ENSP00000516674.1:p.Glu291Thr
ENST00000706955.1:c.*906_*908delinsACT	ENSP00000516675.1:n.*906_*908delinsACT
ENST00000686459.1:c.*457_*459delinsACT	ENSP00000508909.1:n.*457_*459delinsACT
ENST00000688158.1:c.*982_*984delinsACT	ENSP00000509254.1:n.*982_*984delinsACT
ENST00000688308.1:c.871_873delinsACT	ENSP00000508752.1:p.Glu291Thr
ENST00000688922.1:c.792_794delinsACT
ENST00000693560.1:c.1390_1392delinsACT	ENSP00000509861.1:p.Glu464Thr
ENST00000371953.8:c.871_873delinsACT MANE Select	ENSP00000361021.3:p.Glu291Thr
ENST00000371953.7:c.871_873delinsACT	ENSP00000361021.3:p.Glu291Thr
ENST00000472832.2:c.298_300delinsACT	ENSP00000483066.1:p.Glu100Thr
NM_000314.5:c.871_873delinsACT	NP_000305.3:p.Glu291Thr
NM_000314.6:c.871_873delinsACT	NP_000305.3:p.Glu291Thr
NM_001304717.2:c.1390_1392delinsACT	NP_001291646.2:p.Glu464Thr
NM_001304718.1:c.280_282delinsACT	NP_001291647.1:p.Glu94Thr
XM_006717926.2:c.826_828delinsACT	XP_006717989.1:p.Glu276Thr
XM_011539981.1:c.871_873delinsACT	XP_011538283.1:p.Glu291Thr
XM_011539982.1:c.775_777delinsACT	XP_011538284.1:p.Glu259Thr
XR_945791.1:n.1441_1443delinsACT
NM_000314.7:c.871_873delinsACT	NP_000305.3:p.Glu291Thr
NM_001304717.5:c.1390_1392delinsACT	NP_001291646.4:p.Glu464Thr
NM_001304718.2:c.280_282delinsACT	NP_001291647.1:p.Glu94Thr
NM_000314.8:c.871_873delinsACT MANE Select	NP_000305.3:p.Glu291Thr