Canonical Allele Identifier: CA891835683

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960988_87960989delinsCT , CM000672.2:g.87960988_87960989delinsCT	GRCh38
NC_000010.10:g.89720745_89720746delinsCT , CM000672.1:g.89720745_89720746delinsCT	GRCh37
NC_000010.9:g.89710725_89710726delinsCT	NCBI36
NG_007466.2:g.102550_102551delinsCT , LRG_311:g.102550_102551delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.989_990delinsCT	ENSP00000514759.2:p.Glu330Ala
ENST00000710265.1:c.896_897delinsCT	ENSP00000518161.1:p.Glu299Ala
ENST00000472832.3:c.896_897delinsCT	ENSP00000483066.2:p.Glu299Ala
ENST00000688158.2:n.1631_1632delinsCT
ENST00000688922.2:c.*726_*727delinsCT	ENSP00000508742.2:n.*726_*727delinsCT
ENST00000700021.1:c.851_852delinsCT	ENSP00000514757.1:p.Glu284Ala
ENST00000700022.1:c.*235_*236delinsCT	ENSP00000514758.1:n.*235_*236delinsCT
ENST00000700023.1:n.2054_2055delinsCT
ENST00000700024.1:n.2288_2289delinsCT
ENST00000700025.1:n.1665_1666delinsCT
ENST00000700026.1:n.533_534delinsCT
ENST00000706954.1:c.896_897delinsCT	ENSP00000516674.1:p.Glu299Ala
ENST00000706955.1:c.*931_*932delinsCT	ENSP00000516675.1:n.*931_*932delinsCT
ENST00000686459.1:c.*482_*483delinsCT	ENSP00000508909.1:n.*482_*483delinsCT
ENST00000688158.1:c.*1007_*1008delinsCT	ENSP00000509254.1:n.*1007_*1008delinsCT
ENST00000688308.1:c.896_897delinsCT	ENSP00000508752.1:p.Glu299Ala
ENST00000688922.1:c.817_818delinsCT
ENST00000693560.1:c.1415_1416delinsCT	ENSP00000509861.1:p.Glu472Ala
ENST00000371953.8:c.896_897delinsCT MANE Select	ENSP00000361021.3:p.Glu299Ala
ENST00000371953.7:c.896_897delinsCT	ENSP00000361021.3:p.Glu299Ala
ENST00000472832.2:c.323_324delinsCT	ENSP00000483066.1:p.Glu108Ala
NM_000314.5:c.896_897delinsCT	NP_000305.3:p.Glu299Ala
NM_000314.6:c.896_897delinsCT	NP_000305.3:p.Glu299Ala
NM_001304717.2:c.1415_1416delinsCT	NP_001291646.2:p.Glu472Ala
NM_001304718.1:c.305_306delinsCT	NP_001291647.1:p.Glu102Ala
XM_006717926.2:c.851_852delinsCT	XP_006717989.1:p.Glu284Ala
XM_011539981.1:c.896_897delinsCT	XP_011538283.1:p.Glu299Ala
XM_011539982.1:c.800_801delinsCT	XP_011538284.1:p.Glu267Ala
XR_945791.1:n.1466_1467delinsCT
NM_000314.7:c.896_897delinsCT	NP_000305.3:p.Glu299Ala
NM_001304717.5:c.1415_1416delinsCT	NP_001291646.4:p.Glu472Ala
NM_001304718.2:c.305_306delinsCT	NP_001291647.1:p.Glu102Ala
NM_000314.8:c.896_897delinsCT MANE Select	NP_000305.3:p.Glu299Ala