Canonical Allele Identifier: CA2740089959

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960978_87960996del , CM000672.2:g.87960978_87960996del	GRCh38
NC_000010.10:g.89720735_89720753del , CM000672.1:g.89720735_89720753del	GRCh37
NC_000010.9:g.89710715_89710733del	NCBI36
NG_007466.2:g.102540_102558del , LRG_311:g.102540_102558del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.979_997del	ENSP00000514759.2:p.Cys327AlafsTer5
ENST00000710265.1:c.886_904del	ENSP00000518161.1:p.Cys296AlafsTer5
ENST00000472832.3:c.886_904del	ENSP00000483066.2:p.Cys296AlafsTer5
ENST00000688158.2:n.1621_1639del
ENST00000688922.2:c.*716_*734del	ENSP00000508742.2:n.*716_*734del
ENST00000700021.1:c.841_859del	ENSP00000514757.1:p.Cys281AlafsTer5
ENST00000700022.1:c.*225_*243del	ENSP00000514758.1:n.*225_*243del
ENST00000700023.1:n.2044_2062del
ENST00000700024.1:n.2278_2296del
ENST00000700025.1:n.1655_1673del
ENST00000700026.1:n.523_541del
ENST00000706954.1:c.886_904del	ENSP00000516674.1:p.Cys296AlafsTer5
ENST00000706955.1:c.*921_*939del	ENSP00000516675.1:n.*921_*939del
ENST00000686459.1:c.*472_*490del	ENSP00000508909.1:n.*472_*490del
ENST00000688158.1:c.*997_*1015del	ENSP00000509254.1:n.*997_*1015del
ENST00000688308.1:c.886_904del	ENSP00000508752.1:p.Cys296AlafsTer5
ENST00000688922.1:c.807_825del
ENST00000693560.1:c.1405_1423del	ENSP00000509861.1:p.Cys469AlafsTer5
ENST00000371953.8:c.886_904del MANE Select	ENSP00000361021.3:p.Cys296AlafsTer5
ENST00000371953.7:c.886_904del	ENSP00000361021.3:p.Cys296AlafsTer5
ENST00000472832.2:c.313_331del	ENSP00000483066.1:p.Cys105AlafsTer5
NM_000314.5:c.886_904del	NP_000305.3:p.Cys296AlafsTer5
NM_000314.6:c.886_904del	NP_000305.3:p.Cys296AlafsTer5
NM_001304717.2:c.1405_1423del	NP_001291646.2:p.Cys469AlafsTer5
NM_001304718.1:c.295_313del	NP_001291647.1:p.Cys99AlafsTer5
XM_006717926.2:c.841_859del	XP_006717989.1:p.Cys281AlafsTer5
XM_011539981.1:c.886_904del	XP_011538283.1:p.Cys296AlafsTer5
XM_011539982.1:c.790_808del	XP_011538284.1:p.Cys264AlafsTer5
XR_945791.1:n.1456_1474del
NM_000314.7:c.886_904del	NP_000305.3:p.Cys296AlafsTer5
NM_001304717.5:c.1405_1423del	NP_001291646.4:p.Cys469AlafsTer5
NM_001304718.2:c.295_313del	NP_001291647.1:p.Cys99AlafsTer5
NM_000314.8:c.886_904del MANE Select	NP_000305.3:p.Cys296AlafsTer5