Canonical Allele Identifier: CA645553759
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM4940

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925556_87931087del , CM000672.2:g.87925556_87931087del GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.208_251del
ENST00000710265.1:c.208_251del
ENST00000472832.3:c.208_251del
ENST00000688158.2:n.943_986del
ENST00000688922.2:c.208_*81del
ENST00000700021.1:c.165-5490_206del
ENST00000700022.1:c.208_251del
ENST00000700029.1:c.42_85del
ENST00000706954.1:c.208_251del
ENST00000706955.1:c.*243_*286del
ENST00000686459.1:c.208_251del
ENST00000688158.1:c.*319_*362del
ENST00000688308.1:c.208_251del
ENST00000688922.1:c.77_172del
ENST00000693560.1:c.727_770del
ENST00000371953.8:c.208_251del
ENST00000371953.7:c.208_251del
ENST00000498703.1:n.34_77del
ENST00000610634.1:c.106_149del
NM_000314.5:c.208_251del
NM_000314.6:c.208_251del
NM_001304717.2:c.727_770del
NM_001304718.1:c.-541-5490_-500del
XM_006717926.2:c.165-5490_206del
XM_011539981.1:c.208_251del
XM_011539982.1:c.112_155del
XR_945789.1:n.920_963del
XR_945790.1:n.920_963del
XR_945791.1:n.920_963del
NM_000314.7:c.208_251del
NM_001304717.5:c.727_770del
NM_001304718.2:c.-541-5490_-500del
NM_000314.8:c.208_251del