Canonical Allele Identifier: CA2579926489

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965302_87965304delinsTGG , CM000672.2:g.87965302_87965304delinsTGG	GRCh38
NC_000010.10:g.89725059_89725061delinsTGG , CM000672.1:g.89725059_89725061delinsTGG	GRCh37
NC_000010.9:g.89715039_89715041delinsTGG	NCBI36
NG_007466.2:g.106864_106866delinsTGG , LRG_311:g.106864_106866delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1135_1137delinsTGG	ENSP00000514759.2:p.Thr379Trp
ENST00000710265.1:c.*71_*73delinsTGG	ENSP00000518161.1:n.*71_*73delinsTGG
ENST00000688158.2:n.1777_1779delinsTGG
ENST00000688922.2:c.*872_*874delinsTGG	ENSP00000508742.2:n.*872_*874delinsTGG
ENST00000700021.1:c.997_999delinsTGG	ENSP00000514757.1:p.Thr333Trp
ENST00000700022.1:c.*381_*383delinsTGG	ENSP00000514758.1:n.*381_*383delinsTGG
ENST00000700023.1:n.2200_2202delinsTGG
ENST00000700024.1:n.2434_2436delinsTGG
ENST00000706954.1:c.1042_1044delinsTGG	ENSP00000516674.1:p.Thr348Trp
ENST00000706955.1:c.*1077_*1079delinsTGG	ENSP00000516675.1:n.*1077_*1079delinsTGG
ENST00000686459.1:c.*628_*630delinsTGG	ENSP00000508909.1:n.*628_*630delinsTGG
ENST00000688158.1:c.*1153_*1155delinsTGG	ENSP00000509254.1:n.*1153_*1155delinsTGG
ENST00000688308.1:c.1042_1044delinsTGG	ENSP00000508752.1:p.Thr348Trp
ENST00000688922.1:c.963_965delinsTGG
ENST00000693560.1:c.1561_1563delinsTGG	ENSP00000509861.1:p.Thr521Trp
ENST00000371953.8:c.1042_1044delinsTGG MANE Select	ENSP00000361021.3:p.Thr348Trp
ENST00000371953.7:c.1042_1044delinsTGG	ENSP00000361021.3:p.Thr348Trp
NM_000314.5:c.1042_1044delinsTGG	NP_000305.3:p.Thr348Trp
NM_000314.6:c.1042_1044delinsTGG	NP_000305.3:p.Thr348Trp
NM_001304717.2:c.1561_1563delinsTGG	NP_001291646.2:p.Thr521Trp
NM_001304718.1:c.451_453delinsTGG	NP_001291647.1:p.Thr151Trp
XM_006717926.2:c.997_999delinsTGG	XP_006717989.1:p.Thr333Trp
XM_011539982.1:c.946_948delinsTGG	XP_011538284.1:p.Thr316Trp
XR_945791.1:n.1612_1614delinsTGG
NM_000314.7:c.1042_1044delinsTGG	NP_000305.3:p.Thr348Trp
NM_001304717.5:c.1561_1563delinsTGG	NP_001291646.4:p.Thr521Trp
NM_001304718.2:c.451_453delinsTGG	NP_001291647.1:p.Thr151Trp
NM_000314.8:c.1042_1044delinsTGG MANE Select	NP_000305.3:p.Thr348Trp