Canonical Allele Identifier: CA2579926756

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960915_87960917del , CM000672.2:g.87960915_87960917del	GRCh38
NC_000010.10:g.89720672_89720674del , CM000672.1:g.89720672_89720674del	GRCh37
NC_000010.9:g.89710652_89710654del	NCBI36
NG_007466.2:g.102477_102479del , LRG_311:g.102477_102479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.916_918del	ENSP00000514759.2:p.Val306del
ENST00000710265.1:c.823_825del	ENSP00000518161.1:p.Val275del
ENST00000472832.3:c.823_825del	ENSP00000483066.2:p.Val275del
ENST00000688158.2:n.1558_1560del
ENST00000688922.2:c.*653_*655del	ENSP00000508742.2:n.*653_*655del
ENST00000700021.1:c.778_780del	ENSP00000514757.1:p.Val260del
ENST00000700022.1:c.*162_*164del	ENSP00000514758.1:n.*162_*164del
ENST00000700023.1:n.1981_1983del
ENST00000700024.1:n.2215_2217del
ENST00000700025.1:n.1592_1594del
ENST00000700026.1:n.460_462del
ENST00000700029.1:c.750_752del
ENST00000706954.1:c.823_825del	ENSP00000516674.1:p.Val275del
ENST00000706955.1:c.*858_*860del	ENSP00000516675.1:n.*858_*860del
ENST00000686459.1:c.*409_*411del	ENSP00000508909.1:n.*409_*411del
ENST00000688158.1:c.*934_*936del	ENSP00000509254.1:n.*934_*936del
ENST00000688308.1:c.823_825del	ENSP00000508752.1:p.Val275del
ENST00000688922.1:c.744_746del
ENST00000693560.1:c.1342_1344del	ENSP00000509861.1:p.Val448del
ENST00000371953.8:c.823_825del MANE Select	ENSP00000361021.3:p.Val275del
ENST00000371953.7:c.823_825del	ENSP00000361021.3:p.Val275del
ENST00000472832.2:c.250_252del	ENSP00000483066.1:p.Val84del
NM_000314.5:c.823_825del	NP_000305.3:p.Val275del
NM_000314.6:c.823_825del	NP_000305.3:p.Val275del
NM_001304717.2:c.1342_1344del	NP_001291646.2:p.Val448del
NM_001304718.1:c.232_234del	NP_001291647.1:p.Val78del
XM_006717926.2:c.778_780del	XP_006717989.1:p.Val260del
XM_011539981.1:c.823_825del	XP_011538283.1:p.Val275del
XM_011539982.1:c.727_729del	XP_011538284.1:p.Val243del
XR_945791.1:n.1393_1395del
NM_000314.7:c.823_825del	NP_000305.3:p.Val275del
NM_001304717.5:c.1342_1344del	NP_001291646.4:p.Val448del
NM_001304718.2:c.232_234del	NP_001291647.1:p.Val78del
NM_000314.8:c.823_825del MANE Select	NP_000305.3:p.Val275del