Canonical Allele Identifier: CA645554076
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM249822

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960881_87960912del , CM000672.2:g.87960881_87960912del GRCh38
NC_000010.10:g.89720638_89720669del , CM000672.1:g.89720638_89720669del GRCh37
NC_000010.9:g.89710618_89710649del NCBI36
NG_007466.2:g.102443_102474del , LRG_311:g.102443_102474del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-13_913del
ENST00000710265.1:c.802-13_820del
ENST00000472832.3:c.802-13_820del
ENST00000688158.2:n.1537-13_1555del
ENST00000688922.2:c.*632-13_*650del
ENST00000700021.1:c.757-13_775del
ENST00000700022.1:c.*141-13_*159del
ENST00000700023.1:n.1960-13_1978del
ENST00000700024.1:n.2194-13_2212del
ENST00000700025.1:n.1571-13_1589del
ENST00000700026.1:n.439-13_457del
ENST00000700029.1:c.729-13_747del
ENST00000706954.1:c.802-13_820del
ENST00000706955.1:c.*837-13_*855del
ENST00000686459.1:c.*388-13_*406del
ENST00000688158.1:c.*913-13_*931del
ENST00000688308.1:c.802-13_820del
ENST00000688922.1:c.723-13_741del
ENST00000693560.1:c.1321-13_1339del
ENST00000371953.8:c.802-13_820del
ENST00000371953.7:c.802-13_820del
ENST00000472832.2:c.229-13_247del
NM_000314.5:c.802-13_820del
NM_000314.6:c.802-13_820del
NM_001304717.2:c.1321-13_1339del
NM_001304718.1:c.211-13_229del
XM_006717926.2:c.757-13_775del
XM_011539981.1:c.802-13_820del
XM_011539982.1:c.706-13_724del
XR_945791.1:n.1372-13_1390del
NM_000314.7:c.802-13_820del
NM_001304717.5:c.1321-13_1339del
NM_001304718.2:c.211-13_229del
NM_000314.8:c.802-13_820del