Canonical Allele Identifier: CA891840652

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894096_87894097delinsCC , CM000672.2:g.87894096_87894097delinsCC	GRCh38
NC_000010.10:g.89653853_89653854delinsCC , CM000672.1:g.89653853_89653854delinsCC	GRCh37
NC_000010.9:g.89643833_89643834delinsCC	NCBI36
NG_007466.2:g.35658_35659delinsCC , LRG_311:g.35658_35659delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.151_152delinsCC	ENSP00000514759.2:p.Asp51Pro
ENST00000710265.1:c.151_152delinsCC	ENSP00000518161.1:p.Asp51Pro
ENST00000472832.3:c.151_152delinsCC	ENSP00000483066.2:p.Asp51Pro
ENST00000688158.2:n.899+13658_899+13659delinsCC
ENST00000688922.2:c.151_152delinsCC	ENSP00000508742.2:p.Asp51Pro
ENST00000700021.1:c.151_152delinsCC	ENSP00000514757.1:p.Asp51Pro
ENST00000700022.1:c.151_152delinsCC	ENSP00000514758.1:p.Asp51Pro
ENST00000706954.1:c.151_152delinsCC	ENSP00000516674.1:p.Asp51Pro
ENST00000706955.1:c.*186_*187delinsCC	ENSP00000516675.1:n.*186_*187delinsCC
ENST00000686459.1:c.151_152delinsCC	ENSP00000508909.1:p.Asp51Pro
ENST00000688158.1:c.*275+13658_*275+13659delinsCC	ENSP00000509254.1:n.*275+13658_*275+13659delinsCC
ENST00000688308.1:c.151_152delinsCC	ENSP00000508752.1:p.Asp51Pro
ENST00000688922.1:c.20_21delinsCC
ENST00000693560.1:c.670_671delinsCC	ENSP00000509861.1:p.Asp224Pro
ENST00000371953.8:c.151_152delinsCC MANE Select	ENSP00000361021.3:p.Asp51Pro
ENST00000371953.7:c.151_152delinsCC	ENSP00000361021.3:p.Asp51Pro
ENST00000462694.1:n.153_154delinsCC
ENST00000610634.1:c.49_50delinsCC	ENSP00000477517.1:p.Asp17Pro
NM_000314.5:c.151_152delinsCC	NP_000305.3:p.Asp51Pro
NM_000314.6:c.151_152delinsCC	NP_000305.3:p.Asp51Pro
NM_001304717.2:c.670_671delinsCC	NP_001291646.2:p.Asp224Pro
NM_001304718.1:c.-555_-554delinsCC	NP_001291647.1:n.-555_-554delinsCC
XM_006717926.2:c.151_152delinsCC	XP_006717989.1:p.Asp51Pro
XM_011539981.1:c.151_152delinsCC	XP_011538283.1:p.Asp51Pro
XM_011539982.1:c.68+13658_68+13659delinsCC	XP_011538284.1:n.68+13658_68+13659delinsCC
XR_945789.1:n.863_864delinsCC
XR_945790.1:n.863_864delinsCC
XR_945791.1:n.863_864delinsCC
NM_000314.7:c.151_152delinsCC	NP_000305.3:p.Asp51Pro
NM_001304717.5:c.670_671delinsCC	NP_001291646.4:p.Asp224Pro
NM_001304718.2:c.-555_-554delinsCC	NP_001291647.1:n.-555_-554delinsCC
NM_000314.8:c.151_152delinsCC MANE Select	NP_000305.3:p.Asp51Pro