Canonical Allele Identifier: CA2579926777

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960944_87960946del , CM000672.2:g.87960944_87960946del	GRCh38
NC_000010.10:g.89720701_89720703del , CM000672.1:g.89720701_89720703del	GRCh37
NC_000010.9:g.89710681_89710683del	NCBI36
NG_007466.2:g.102506_102508del , LRG_311:g.102506_102508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.945_947del	ENSP00000514759.2:p.Glu316del
ENST00000710265.1:c.852_854del	ENSP00000518161.1:p.Glu285del
ENST00000472832.3:c.852_854del	ENSP00000483066.2:p.Glu285del
ENST00000688158.2:n.1587_1589del
ENST00000688922.2:c.*682_*684del	ENSP00000508742.2:n.*682_*684del
ENST00000700021.1:c.807_809del	ENSP00000514757.1:p.Glu270del
ENST00000700022.1:c.*191_*193del	ENSP00000514758.1:n.*191_*193del
ENST00000700023.1:n.2010_2012del
ENST00000700024.1:n.2244_2246del
ENST00000700025.1:n.1621_1623del
ENST00000700026.1:n.489_491del
ENST00000700029.1:c.779_781del
ENST00000706954.1:c.852_854del	ENSP00000516674.1:p.Glu285del
ENST00000706955.1:c.*887_*889del	ENSP00000516675.1:n.*887_*889del
ENST00000686459.1:c.*438_*440del	ENSP00000508909.1:n.*438_*440del
ENST00000688158.1:c.*963_*965del	ENSP00000509254.1:n.*963_*965del
ENST00000688308.1:c.852_854del	ENSP00000508752.1:p.Glu285del
ENST00000688922.1:c.773_775del
ENST00000693560.1:c.1371_1373del	ENSP00000509861.1:p.Glu458del
ENST00000371953.8:c.852_854del MANE Select	ENSP00000361021.3:p.Glu285del
ENST00000371953.7:c.852_854del	ENSP00000361021.3:p.Glu285del
ENST00000472832.2:c.279_281del	ENSP00000483066.1:p.Glu94del
NM_000314.5:c.852_854del	NP_000305.3:p.Glu285del
NM_000314.6:c.852_854del	NP_000305.3:p.Glu285del
NM_001304717.2:c.1371_1373del	NP_001291646.2:p.Glu458del
NM_001304718.1:c.261_263del	NP_001291647.1:p.Glu88del
XM_006717926.2:c.807_809del	XP_006717989.1:p.Glu270del
XM_011539981.1:c.852_854del	XP_011538283.1:p.Glu285del
XM_011539982.1:c.756_758del	XP_011538284.1:p.Glu253del
XR_945791.1:n.1422_1424del
NM_000314.7:c.852_854del	NP_000305.3:p.Glu285del
NM_001304717.5:c.1371_1373del	NP_001291646.4:p.Glu458del
NM_001304718.2:c.261_263del	NP_001291647.1:p.Glu88del
NM_000314.8:c.852_854del MANE Select	NP_000305.3:p.Glu285del