Canonical Allele Identifier: CA1926175382

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933157_87933162delinsTAATGA , CM000672.2:g.87933157_87933162delinsTAATGA	GRCh38
NC_000010.10:g.89692914_89692919delinsTAATGA , CM000672.1:g.89692914_89692919delinsTAATGA	GRCh37
NC_000010.9:g.89682894_89682899delinsTAATGA	NCBI36
NG_007466.2:g.74719_74724delinsTAATGA , LRG_311:g.74719_74724delinsTAATGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.398_403delinsTAATGA	ENSP00000514759.2:p.Val133=
ENST00000710265.1:c.398_403delinsTAATGA	ENSP00000518161.1:p.Val133=
ENST00000472832.3:c.398_403delinsTAATGA	ENSP00000483066.2:p.Val133=
ENST00000688158.2:n.1133_1138delinsTAATGA
ENST00000688922.2:c.*228_*233delinsTAATGA	ENSP00000508742.2:n.*228_*233delinsTAATGA
ENST00000700021.1:c.353_358delinsTAATGA	ENSP00000514757.1:p.Val118=
ENST00000700022.1:c.398_403delinsTAATGA	ENSP00000514758.1:p.Val133=
ENST00000700029.1:c.232_237delinsTAATGA
ENST00000706954.1:c.398_403delinsTAATGA	ENSP00000516674.1:p.Val133=
ENST00000706955.1:c.*433_*438delinsTAATGA	ENSP00000516675.1:n.*433_*438delinsTAATGA
ENST00000686459.1:c.398_403delinsTAATGA	ENSP00000508909.1:p.Val133=
ENST00000688158.1:c.*509_*514delinsTAATGA	ENSP00000509254.1:n.*509_*514delinsTAATGA
ENST00000688308.1:c.398_403delinsTAATGA	ENSP00000508752.1:p.Val133=
ENST00000688922.1:c.319_324delinsTAATGA
ENST00000693560.1:c.917_922delinsTAATGA	ENSP00000509861.1:p.Val306=
ENST00000371953.8:c.398_403delinsTAATGA MANE Select	ENSP00000361021.3:p.Val133=
ENST00000371953.7:c.398_403delinsTAATGA	ENSP00000361021.3:p.Val133=
ENST00000498703.1:n.224_229delinsTAATGA
ENST00000610634.1:c.296_301delinsTAATGA	ENSP00000477517.1:p.Val99=
NM_000314.5:c.398_403delinsTAATGA	NP_000305.3:p.Val133=
NM_000314.6:c.398_403delinsTAATGA	NP_000305.3:p.Val133=
NM_001304717.2:c.917_922delinsTAATGA	NP_001291646.2:p.Val306=
NM_001304718.1:c.-353_-348delinsTAATGA	NP_001291647.1:n.-353_-348delinsTAATGA
XM_006717926.2:c.353_358delinsTAATGA	XP_006717989.1:p.Val118=
XM_011539981.1:c.398_403delinsTAATGA	XP_011538283.1:p.Val133=
XM_011539982.1:c.302_307delinsTAATGA	XP_011538284.1:p.Val101=
XR_945789.1:n.1110_1115delinsTAATGA
XR_945790.1:n.1110_1115delinsTAATGA
XR_945791.1:n.1110_1115delinsTAATGA
NM_000314.7:c.398_403delinsTAATGA	NP_000305.3:p.Val133=
NM_001304717.5:c.917_922delinsTAATGA	NP_001291646.4:p.Val306=
NM_001304718.2:c.-353_-348delinsTAATGA	NP_001291647.1:n.-353_-348delinsTAATGA
NM_000314.8:c.398_403delinsTAATGA MANE Select	NP_000305.3:p.Val133=