Canonical Allele Identifier: CA891835687

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960988_87960989delinsGT , CM000672.2:g.87960988_87960989delinsGT	GRCh38
NC_000010.10:g.89720745_89720746delinsGT , CM000672.1:g.89720745_89720746delinsGT	GRCh37
NC_000010.9:g.89710725_89710726delinsGT	NCBI36
NG_007466.2:g.102550_102551delinsGT , LRG_311:g.102550_102551delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.989_990delinsGT	ENSP00000514759.2:p.Glu330Gly
ENST00000710265.1:c.896_897delinsGT	ENSP00000518161.1:p.Glu299Gly
ENST00000472832.3:c.896_897delinsGT	ENSP00000483066.2:p.Glu299Gly
ENST00000688158.2:n.1631_1632delinsGT
ENST00000688922.2:c.*726_*727delinsGT	ENSP00000508742.2:n.*726_*727delinsGT
ENST00000700021.1:c.851_852delinsGT	ENSP00000514757.1:p.Glu284Gly
ENST00000700022.1:c.*235_*236delinsGT	ENSP00000514758.1:n.*235_*236delinsGT
ENST00000700023.1:n.2054_2055delinsGT
ENST00000700024.1:n.2288_2289delinsGT
ENST00000700025.1:n.1665_1666delinsGT
ENST00000700026.1:n.533_534delinsGT
ENST00000706954.1:c.896_897delinsGT	ENSP00000516674.1:p.Glu299Gly
ENST00000706955.1:c.*931_*932delinsGT	ENSP00000516675.1:n.*931_*932delinsGT
ENST00000686459.1:c.*482_*483delinsGT	ENSP00000508909.1:n.*482_*483delinsGT
ENST00000688158.1:c.*1007_*1008delinsGT	ENSP00000509254.1:n.*1007_*1008delinsGT
ENST00000688308.1:c.896_897delinsGT	ENSP00000508752.1:p.Glu299Gly
ENST00000688922.1:c.817_818delinsGT
ENST00000693560.1:c.1415_1416delinsGT	ENSP00000509861.1:p.Glu472Gly
ENST00000371953.8:c.896_897delinsGT MANE Select	ENSP00000361021.3:p.Glu299Gly
ENST00000371953.7:c.896_897delinsGT	ENSP00000361021.3:p.Glu299Gly
ENST00000472832.2:c.323_324delinsGT	ENSP00000483066.1:p.Glu108Gly
NM_000314.5:c.896_897delinsGT	NP_000305.3:p.Glu299Gly
NM_000314.6:c.896_897delinsGT	NP_000305.3:p.Glu299Gly
NM_001304717.2:c.1415_1416delinsGT	NP_001291646.2:p.Glu472Gly
NM_001304718.1:c.305_306delinsGT	NP_001291647.1:p.Glu102Gly
XM_006717926.2:c.851_852delinsGT	XP_006717989.1:p.Glu284Gly
XM_011539981.1:c.896_897delinsGT	XP_011538283.1:p.Glu299Gly
XM_011539982.1:c.800_801delinsGT	XP_011538284.1:p.Glu267Gly
XR_945791.1:n.1466_1467delinsGT
NM_000314.7:c.896_897delinsGT	NP_000305.3:p.Glu299Gly
NM_001304717.5:c.1415_1416delinsGT	NP_001291646.4:p.Glu472Gly
NM_001304718.2:c.305_306delinsGT	NP_001291647.1:p.Glu102Gly
NM_000314.8:c.896_897delinsGT MANE Select	NP_000305.3:p.Glu299Gly