Canonical Allele Identifier: CA645553780

Gene: PTEN

Linked Data

• COSMIC: COSM4968

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87931080_87933044del , CM000672.2:g.87931080_87933044del	GRCh38
NC_000010.10:g.89690837_89692801del , CM000672.1:g.89690837_89692801del	GRCh37
NC_000010.9:g.89680817_89682781del	NCBI36
NG_007466.2:g.72642_74606del , LRG_311:g.72642_74606del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.244_285del
ENST00000710265.1:c.244_285del
ENST00000472832.3:c.244_285del
ENST00000688158.2:n.979_1020del
ENST00000688922.2:c.*74_*115del
ENST00000700021.1:c.199_240del
ENST00000700022.1:c.244_285del
ENST00000700029.1:c.78_119del
ENST00000706954.1:c.244_285del
ENST00000706955.1:c.*279_*320del
ENST00000686459.1:c.244_285del
ENST00000688158.1:c.*355_*396del
ENST00000688308.1:c.244_285del
ENST00000688922.1:c.165_206del
ENST00000693560.1:c.763_804del
ENST00000371953.8:c.244_285del
ENST00000371953.7:c.244_285del
ENST00000498703.1:n.70_111del
ENST00000610634.1:c.142_183del
NM_000314.5:c.244_285del
NM_000314.6:c.244_285del
NM_001304717.2:c.763_804del
NM_001304718.1:c.-507_-466del
XM_006717926.2:c.199_240del
XM_011539981.1:c.244_285del
XM_011539982.1:c.148_189del
XR_945789.1:n.956_997del
XR_945790.1:n.956_997del
XR_945791.1:n.956_997del
NM_000314.7:c.244_285del
NM_001304717.5:c.763_804del
NM_001304718.2:c.-507_-466del
NM_000314.8:c.244_285del