Canonical Allele Identifier: CA645554069

Gene: PTEN

Linked Data

• COSMIC: COSM4890

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958010_87960896del , CM000672.2:g.87958010_87960896del	GRCh38
NC_000010.10:g.89717767_89720653del , CM000672.1:g.89717767_89720653del	GRCh37
NC_000010.9:g.89707747_89710633del	NCBI36
NG_007466.2:g.99572_102458del , LRG_311:g.99572_102458del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.792_897del
ENST00000710265.1:c.792_804del
ENST00000472832.3:c.792_804del
ENST00000688158.2:n.1527_1539del
ENST00000688922.2:c.*622_*634del
ENST00000700021.1:c.747_759del
ENST00000700022.1:c.*131_*143del
ENST00000700023.1:n.1950_1962del
ENST00000700024.1:n.2184_2196del
ENST00000700025.1:n.1561_1573del
ENST00000700026.1:n.429_441del
ENST00000700029.1:c.626_731del
ENST00000706954.1:c.792_804del
ENST00000706955.1:c.*827_*839del
ENST00000686459.1:c.*378_*390del
ENST00000688158.1:c.*903_*915del
ENST00000688308.1:c.792_804del
ENST00000688922.1:c.713_725del
ENST00000693560.1:c.1311_1323del
ENST00000371953.8:c.792_804del
ENST00000371953.7:c.792_804del
ENST00000472832.2:c.219_231del
NM_000314.5:c.792_804del
NM_000314.6:c.792_804del
NM_001304717.2:c.1311_1323del
NM_001304718.1:c.201_213del
XM_006717926.2:c.747_759del
XM_011539981.1:c.792_804del
XM_011539982.1:c.696_708del
XR_945791.1:n.1362_1374del
NM_000314.7:c.792_804del
NM_001304717.5:c.1311_1323del
NM_001304718.2:c.201_213del
NM_000314.8:c.792_804del