Canonical Allele Identifier: CA891835195

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894079_87894080delinsCT , CM000672.2:g.87894079_87894080delinsCT	GRCh38
NC_000010.10:g.89653836_89653837delinsCT , CM000672.1:g.89653836_89653837delinsCT	GRCh37
NC_000010.9:g.89643816_89643817delinsCT	NCBI36
NG_007466.2:g.35641_35642delinsCT , LRG_311:g.35641_35642delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.134_135delinsCT	ENSP00000514759.2:p.Val45Ala
ENST00000710265.1:c.134_135delinsCT	ENSP00000518161.1:p.Val45Ala
ENST00000472832.3:c.134_135delinsCT	ENSP00000483066.2:p.Val45Ala
ENST00000688158.2:n.899+13641_899+13642delinsCT
ENST00000688922.2:c.134_135delinsCT	ENSP00000508742.2:p.Val45Ala
ENST00000700021.1:c.134_135delinsCT	ENSP00000514757.1:p.Val45Ala
ENST00000700022.1:c.134_135delinsCT	ENSP00000514758.1:p.Val45Ala
ENST00000706954.1:c.134_135delinsCT	ENSP00000516674.1:p.Val45Ala
ENST00000706955.1:c.*169_*170delinsCT	ENSP00000516675.1:n.*169_*170delinsCT
ENST00000686459.1:c.134_135delinsCT	ENSP00000508909.1:p.Val45Ala
ENST00000688158.1:c.*275+13641_*275+13642delinsCT	ENSP00000509254.1:n.*275+13641_*275+13642delinsCT
ENST00000688308.1:c.134_135delinsCT	ENSP00000508752.1:p.Val45Ala
ENST00000688922.1:c.3_4delinsCT
ENST00000693560.1:c.653_654delinsCT	ENSP00000509861.1:p.Val218Ala
ENST00000371953.8:c.134_135delinsCT MANE Select	ENSP00000361021.3:p.Val45Ala
ENST00000371953.7:c.134_135delinsCT	ENSP00000361021.3:p.Val45Ala
ENST00000462694.1:n.136_137delinsCT
ENST00000610634.1:c.32_33delinsCT	ENSP00000477517.1:p.Val11Ala
NM_000314.5:c.134_135delinsCT	NP_000305.3:p.Val45Ala
NM_000314.6:c.134_135delinsCT	NP_000305.3:p.Val45Ala
NM_001304717.2:c.653_654delinsCT	NP_001291646.2:p.Val218Ala
NM_001304718.1:c.-572_-571delinsCT	NP_001291647.1:n.-572_-571delinsCT
XM_006717926.2:c.134_135delinsCT	XP_006717989.1:p.Val45Ala
XM_011539981.1:c.134_135delinsCT	XP_011538283.1:p.Val45Ala
XM_011539982.1:c.68+13641_68+13642delinsCT	XP_011538284.1:n.68+13641_68+13642delinsCT
XR_945789.1:n.846_847delinsCT
XR_945790.1:n.846_847delinsCT
XR_945791.1:n.846_847delinsCT
NM_000314.7:c.134_135delinsCT	NP_000305.3:p.Val45Ala
NM_001304717.5:c.653_654delinsCT	NP_001291646.4:p.Val218Ala
NM_001304718.2:c.-572_-571delinsCT	NP_001291647.1:n.-572_-571delinsCT
NM_000314.8:c.134_135delinsCT MANE Select	NP_000305.3:p.Val45Ala