Canonical Allele Identifier: CA891841027

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960915_87960917delinsCAT , CM000672.2:g.87960915_87960917delinsCAT	GRCh38
NC_000010.10:g.89720672_89720674delinsCAT , CM000672.1:g.89720672_89720674delinsCAT	GRCh37
NC_000010.9:g.89710652_89710654delinsCAT	NCBI36
NG_007466.2:g.102477_102479delinsCAT , LRG_311:g.102477_102479delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.916_918delinsCAT	ENSP00000514759.2:p.Val306His
ENST00000710265.1:c.823_825delinsCAT	ENSP00000518161.1:p.Val275His
ENST00000472832.3:c.823_825delinsCAT	ENSP00000483066.2:p.Val275His
ENST00000688158.2:n.1558_1560delinsCAT
ENST00000688922.2:c.*653_*655delinsCAT	ENSP00000508742.2:n.*653_*655delinsCAT
ENST00000700021.1:c.778_780delinsCAT	ENSP00000514757.1:p.Val260His
ENST00000700022.1:c.*162_*164delinsCAT	ENSP00000514758.1:n.*162_*164delinsCAT
ENST00000700023.1:n.1981_1983delinsCAT
ENST00000700024.1:n.2215_2217delinsCAT
ENST00000700025.1:n.1592_1594delinsCAT
ENST00000700026.1:n.460_462delinsCAT
ENST00000700029.1:c.750_752delinsCAT
ENST00000706954.1:c.823_825delinsCAT	ENSP00000516674.1:p.Val275His
ENST00000706955.1:c.*858_*860delinsCAT	ENSP00000516675.1:n.*858_*860delinsCAT
ENST00000686459.1:c.*409_*411delinsCAT	ENSP00000508909.1:n.*409_*411delinsCAT
ENST00000688158.1:c.*934_*936delinsCAT	ENSP00000509254.1:n.*934_*936delinsCAT
ENST00000688308.1:c.823_825delinsCAT	ENSP00000508752.1:p.Val275His
ENST00000688922.1:c.744_746delinsCAT
ENST00000693560.1:c.1342_1344delinsCAT	ENSP00000509861.1:p.Val448His
ENST00000371953.8:c.823_825delinsCAT MANE Select	ENSP00000361021.3:p.Val275His
ENST00000371953.7:c.823_825delinsCAT	ENSP00000361021.3:p.Val275His
ENST00000472832.2:c.250_252delinsCAT	ENSP00000483066.1:p.Val84His
NM_000314.5:c.823_825delinsCAT	NP_000305.3:p.Val275His
NM_000314.6:c.823_825delinsCAT	NP_000305.3:p.Val275His
NM_001304717.2:c.1342_1344delinsCAT	NP_001291646.2:p.Val448His
NM_001304718.1:c.232_234delinsCAT	NP_001291647.1:p.Val78His
XM_006717926.2:c.778_780delinsCAT	XP_006717989.1:p.Val260His
XM_011539981.1:c.823_825delinsCAT	XP_011538283.1:p.Val275His
XM_011539982.1:c.727_729delinsCAT	XP_011538284.1:p.Val243His
XR_945791.1:n.1393_1395delinsCAT
NM_000314.7:c.823_825delinsCAT	NP_000305.3:p.Val275His
NM_001304717.5:c.1342_1344delinsCAT	NP_001291646.4:p.Val448His
NM_001304718.2:c.232_234delinsCAT	NP_001291647.1:p.Val78His
NM_000314.8:c.823_825delinsCAT MANE Select	NP_000305.3:p.Val275His