Canonical Allele Identifier: CA891835238

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960963_87960965delinsAAT , CM000672.2:g.87960963_87960965delinsAAT	GRCh38
NC_000010.10:g.89720720_89720722delinsAAT , CM000672.1:g.89720720_89720722delinsAAT	GRCh37
NC_000010.9:g.89710700_89710702delinsAAT	NCBI36
NG_007466.2:g.102525_102527delinsAAT , LRG_311:g.102525_102527delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.964_966delinsAAT	ENSP00000514759.2:p.Glu322Asn
ENST00000710265.1:c.871_873delinsAAT	ENSP00000518161.1:p.Glu291Asn
ENST00000472832.3:c.871_873delinsAAT	ENSP00000483066.2:p.Glu291Asn
ENST00000688158.2:n.1606_1608delinsAAT
ENST00000688922.2:c.*701_*703delinsAAT	ENSP00000508742.2:n.*701_*703delinsAAT
ENST00000700021.1:c.826_828delinsAAT	ENSP00000514757.1:p.Glu276Asn
ENST00000700022.1:c.*210_*212delinsAAT	ENSP00000514758.1:n.*210_*212delinsAAT
ENST00000700023.1:n.2029_2031delinsAAT
ENST00000700024.1:n.2263_2265delinsAAT
ENST00000700025.1:n.1640_1642delinsAAT
ENST00000700026.1:n.508_510delinsAAT
ENST00000700029.1:c.798_800delinsAAT
ENST00000706954.1:c.871_873delinsAAT	ENSP00000516674.1:p.Glu291Asn
ENST00000706955.1:c.*906_*908delinsAAT	ENSP00000516675.1:n.*906_*908delinsAAT
ENST00000686459.1:c.*457_*459delinsAAT	ENSP00000508909.1:n.*457_*459delinsAAT
ENST00000688158.1:c.*982_*984delinsAAT	ENSP00000509254.1:n.*982_*984delinsAAT
ENST00000688308.1:c.871_873delinsAAT	ENSP00000508752.1:p.Glu291Asn
ENST00000688922.1:c.792_794delinsAAT
ENST00000693560.1:c.1390_1392delinsAAT	ENSP00000509861.1:p.Glu464Asn
ENST00000371953.8:c.871_873delinsAAT MANE Select	ENSP00000361021.3:p.Glu291Asn
ENST00000371953.7:c.871_873delinsAAT	ENSP00000361021.3:p.Glu291Asn
ENST00000472832.2:c.298_300delinsAAT	ENSP00000483066.1:p.Glu100Asn
NM_000314.5:c.871_873delinsAAT	NP_000305.3:p.Glu291Asn
NM_000314.6:c.871_873delinsAAT	NP_000305.3:p.Glu291Asn
NM_001304717.2:c.1390_1392delinsAAT	NP_001291646.2:p.Glu464Asn
NM_001304718.1:c.280_282delinsAAT	NP_001291647.1:p.Glu94Asn
XM_006717926.2:c.826_828delinsAAT	XP_006717989.1:p.Glu276Asn
XM_011539981.1:c.871_873delinsAAT	XP_011538283.1:p.Glu291Asn
XM_011539982.1:c.775_777delinsAAT	XP_011538284.1:p.Glu259Asn
XR_945791.1:n.1441_1443delinsAAT
NM_000314.7:c.871_873delinsAAT	NP_000305.3:p.Glu291Asn
NM_001304717.5:c.1390_1392delinsAAT	NP_001291646.4:p.Glu464Asn
NM_001304718.2:c.280_282delinsAAT	NP_001291647.1:p.Glu94Asn
NM_000314.8:c.871_873delinsAAT MANE Select	NP_000305.3:p.Glu291Asn