Canonical Allele Identifier: CA645553835

Gene: PTEN

Linked Data

• COSMIC: COSM4946

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933151_87933170del , CM000672.2:g.87933151_87933170del	GRCh38
NC_000010.10:g.89692908_89692927del , CM000672.1:g.89692908_89692927del	GRCh37
NC_000010.9:g.89682888_89682907del	NCBI36
NG_007466.2:g.74713_74732del , LRG_311:g.74713_74732del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.392_411del	ENSP00000514759.2:p.Thr131IlefsTer?
ENST00000710265.1:c.392_411del	ENSP00000518161.1:p.Thr131IlefsTer?
ENST00000472832.3:c.392_411del	ENSP00000483066.2:p.Thr131IlefsTer?
ENST00000688158.2:n.1127_1146del
ENST00000688922.2:c.*222_*241del	ENSP00000508742.2:n.*222_*241del
ENST00000700021.1:c.347_366del	ENSP00000514757.1:p.Thr116IlefsTer?
ENST00000700022.1:c.392_411del	ENSP00000514758.1:p.Thr131IlefsTer?
ENST00000700029.1:c.226_245del
ENST00000706954.1:c.392_411del	ENSP00000516674.1:p.Thr131IlefsTer?
ENST00000706955.1:c.*427_*446del	ENSP00000516675.1:n.*427_*446del
ENST00000686459.1:c.392_411del	ENSP00000508909.1:p.Thr131IlefsTer?
ENST00000688158.1:c.*503_*522del	ENSP00000509254.1:n.*503_*522del
ENST00000688308.1:c.392_411del	ENSP00000508752.1:p.Thr131IlefsTer?
ENST00000688922.1:c.313_332del
ENST00000693560.1:c.911_930del	ENSP00000509861.1:p.Thr304IlefsTer?
ENST00000371953.8:c.392_411del MANE Select	ENSP00000361021.3:p.Thr131IlefsTer?
ENST00000371953.7:c.392_411del	ENSP00000361021.3:p.Thr131IlefsTer?
ENST00000498703.1:n.218_237del
ENST00000610634.1:c.290_309del	ENSP00000477517.1:p.Thr97IlefsTer?
NM_000314.5:c.392_411del	NP_000305.3:p.Thr131IlefsTer?
NM_000314.6:c.392_411del	NP_000305.3:p.Thr131IlefsTer?
NM_001304717.2:c.911_930del	NP_001291646.2:p.Thr304IlefsTer?
NM_001304718.1:c.-359_-340del	NP_001291647.1:n.-359_-340del
XM_006717926.2:c.347_366del	XP_006717989.1:p.Thr116IlefsTer?
XM_011539981.1:c.392_411del	XP_011538283.1:p.Thr131IlefsTer?
XM_011539982.1:c.296_315del	XP_011538284.1:p.Thr99IlefsTer?
XR_945789.1:n.1104_1123del
XR_945790.1:n.1104_1123del
XR_945791.1:n.1104_1123del
NM_000314.7:c.392_411del	NP_000305.3:p.Thr131IlefsTer?
NM_001304717.5:c.911_930del	NP_001291646.4:p.Thr304IlefsTer?
NM_001304718.2:c.-359_-340del	NP_001291647.1:n.-359_-340del
NM_000314.8:c.392_411del MANE Select	NP_000305.3:p.Thr131IlefsTer?