Canonical Allele Identifier: CA891840260

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960916_87960917delinsGT , CM000672.2:g.87960916_87960917delinsGT	GRCh38
NC_000010.10:g.89720673_89720674delinsGT , CM000672.1:g.89720673_89720674delinsGT	GRCh37
NC_000010.9:g.89710653_89710654delinsGT	NCBI36
NG_007466.2:g.102478_102479delinsGT , LRG_311:g.102478_102479delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.917_918delinsGT	ENSP00000514759.2:p.Val306Gly
ENST00000710265.1:c.824_825delinsGT	ENSP00000518161.1:p.Val275Gly
ENST00000472832.3:c.824_825delinsGT	ENSP00000483066.2:p.Val275Gly
ENST00000688158.2:n.1559_1560delinsGT
ENST00000688922.2:c.*654_*655delinsGT	ENSP00000508742.2:n.*654_*655delinsGT
ENST00000700021.1:c.779_780delinsGT	ENSP00000514757.1:p.Val260Gly
ENST00000700022.1:c.*163_*164delinsGT	ENSP00000514758.1:n.*163_*164delinsGT
ENST00000700023.1:n.1982_1983delinsGT
ENST00000700024.1:n.2216_2217delinsGT
ENST00000700025.1:n.1593_1594delinsGT
ENST00000700026.1:n.461_462delinsGT
ENST00000700029.1:c.751_752delinsGT
ENST00000706954.1:c.824_825delinsGT	ENSP00000516674.1:p.Val275Gly
ENST00000706955.1:c.*859_*860delinsGT	ENSP00000516675.1:n.*859_*860delinsGT
ENST00000686459.1:c.*410_*411delinsGT	ENSP00000508909.1:n.*410_*411delinsGT
ENST00000688158.1:c.*935_*936delinsGT	ENSP00000509254.1:n.*935_*936delinsGT
ENST00000688308.1:c.824_825delinsGT	ENSP00000508752.1:p.Val275Gly
ENST00000688922.1:c.745_746delinsGT
ENST00000693560.1:c.1343_1344delinsGT	ENSP00000509861.1:p.Val448Gly
ENST00000371953.8:c.824_825delinsGT MANE Select	ENSP00000361021.3:p.Val275Gly
ENST00000371953.7:c.824_825delinsGT	ENSP00000361021.3:p.Val275Gly
ENST00000472832.2:c.251_252delinsGT	ENSP00000483066.1:p.Val84Gly
NM_000314.5:c.824_825delinsGT	NP_000305.3:p.Val275Gly
NM_000314.6:c.824_825delinsGT	NP_000305.3:p.Val275Gly
NM_001304717.2:c.1343_1344delinsGT	NP_001291646.2:p.Val448Gly
NM_001304718.1:c.233_234delinsGT	NP_001291647.1:p.Val78Gly
XM_006717926.2:c.779_780delinsGT	XP_006717989.1:p.Val260Gly
XM_011539981.1:c.824_825delinsGT	XP_011538283.1:p.Val275Gly
XM_011539982.1:c.728_729delinsGT	XP_011538284.1:p.Val243Gly
XR_945791.1:n.1394_1395delinsGT
NM_000314.7:c.824_825delinsGT	NP_000305.3:p.Val275Gly
NM_001304717.5:c.1343_1344delinsGT	NP_001291646.4:p.Val448Gly
NM_001304718.2:c.233_234delinsGT	NP_001291647.1:p.Val78Gly
NM_000314.8:c.824_825delinsGT MANE Select	NP_000305.3:p.Val275Gly