Canonical Allele Identifier: CA645559019

Gene: PTEN

Linked Data

• COSMIC: COSM5016

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894079_87894080insCA , CM000672.2:g.87894079_87894080insCA	GRCh38
NC_000010.10:g.89653836_89653837insCA , CM000672.1:g.89653836_89653837insCA	GRCh37
NC_000010.9:g.89643816_89643817insCA	NCBI36
NG_007466.2:g.35641_35642insCA , LRG_311:g.35641_35642insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.134_135insCA	ENSP00000514759.2:p.Tyr46AsnfsTer9
ENST00000710265.1:c.134_135insCA	ENSP00000518161.1:p.Tyr46AsnfsTer9
ENST00000472832.3:c.134_135insCA	ENSP00000483066.2:p.Tyr46AsnfsTer9
ENST00000688158.2:n.899+13641_899+13642insCA
ENST00000688922.2:c.134_135insCA	ENSP00000508742.2:p.Tyr46AsnfsTer9
ENST00000700021.1:c.134_135insCA	ENSP00000514757.1:p.Tyr46AsnfsTer9
ENST00000700022.1:c.134_135insCA	ENSP00000514758.1:p.Tyr46AsnfsTer9
ENST00000706954.1:c.134_135insCA	ENSP00000516674.1:p.Tyr46AsnfsTer9
ENST00000706955.1:c.*169_*170insCA	ENSP00000516675.1:n.*169_*170insCA
ENST00000686459.1:c.134_135insCA	ENSP00000508909.1:p.Tyr46AsnfsTer9
ENST00000688158.1:c.*275+13641_*275+13642insCA	ENSP00000509254.1:n.*275+13641_*275+13642insCA
ENST00000688308.1:c.134_135insCA	ENSP00000508752.1:p.Tyr46AsnfsTer9
ENST00000688922.1:c.3_4insCA
ENST00000693560.1:c.653_654insCA	ENSP00000509861.1:p.Tyr219AsnfsTer9
ENST00000371953.8:c.134_135insCA MANE Select	ENSP00000361021.3:p.Tyr46AsnfsTer9
ENST00000371953.7:c.134_135insCA	ENSP00000361021.3:p.Tyr46AsnfsTer9
ENST00000462694.1:n.136_137insCA
ENST00000610634.1:c.32_33insCA	ENSP00000477517.1:p.Tyr12AsnfsTer9
NM_000314.5:c.134_135insCA	NP_000305.3:p.Tyr46AsnfsTer9
NM_000314.6:c.134_135insCA	NP_000305.3:p.Tyr46AsnfsTer9
NM_001304717.2:c.653_654insCA	NP_001291646.2:p.Tyr219AsnfsTer9
NM_001304718.1:c.-572_-571insCA	NP_001291647.1:n.-572_-571insCA
XM_006717926.2:c.134_135insCA	XP_006717989.1:p.Tyr46AsnfsTer9
XM_011539981.1:c.134_135insCA	XP_011538283.1:p.Tyr46AsnfsTer9
XM_011539982.1:c.68+13641_68+13642insCA	XP_011538284.1:n.68+13641_68+13642insCA
XR_945789.1:n.846_847insCA
XR_945790.1:n.846_847insCA
XR_945791.1:n.846_847insCA
NM_000314.7:c.134_135insCA	NP_000305.3:p.Tyr46AsnfsTer9
NM_001304717.5:c.653_654insCA	NP_001291646.4:p.Tyr219AsnfsTer9
NM_001304718.2:c.-572_-571insCA	NP_001291647.1:n.-572_-571insCA
NM_000314.8:c.134_135insCA MANE Select	NP_000305.3:p.Tyr46AsnfsTer9