Canonical Allele Identifier: CA2499220470
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132281665

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960891_87960896del , CM000672.2:g.87960891_87960896del GRCh38
NC_000010.10:g.89720648_89720653del , CM000672.1:g.89720648_89720653del GRCh37
NC_000010.9:g.89710628_89710633del NCBI36
NG_007466.2:g.102453_102458del , LRG_311:g.102453_102458del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-3_897del
ENST00000710265.1:c.802-3_804del
ENST00000472832.3:c.802-3_804del
ENST00000688158.2:n.1537-3_1539del
ENST00000688922.2:c.*632-3_*634del
ENST00000700021.1:c.757-3_759del
ENST00000700022.1:c.*141-3_*143del
ENST00000700023.1:n.1960-3_1962del
ENST00000700024.1:n.2194-3_2196del
ENST00000700025.1:n.1571-3_1573del
ENST00000700026.1:n.439-3_441del
ENST00000700029.1:c.729-3_731del
ENST00000706954.1:c.802-3_804del
ENST00000706955.1:c.*837-3_*839del
ENST00000686459.1:c.*388-3_*390del
ENST00000688158.1:c.*913-3_*915del
ENST00000688308.1:c.802-3_804del
ENST00000688922.1:c.723-3_725del
ENST00000693560.1:c.1321-3_1323del
ENST00000371953.8:c.802-3_804del
ENST00000371953.7:c.802-3_804del
ENST00000472832.2:c.229-3_231del
NM_000314.5:c.802-3_804del
NM_000314.6:c.802-3_804del
NM_001304717.2:c.1321-3_1323del
NM_001304718.1:c.211-3_213del
XM_006717926.2:c.757-3_759del
XM_011539981.1:c.802-3_804del
XM_011539982.1:c.706-3_708del
XR_945791.1:n.1372-3_1374del
NM_000314.7:c.802-3_804del
NM_001304717.5:c.1321-3_1323del
NM_001304718.2:c.211-3_213del
NM_000314.8:c.802-3_804del