Canonical Allele Identifier: CA645554078

Gene: PTEN

Linked Data

• COSMIC: COSM3737052

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960891_87960894dup , CM000672.2:g.87960891_87960894dup	GRCh38
NC_000010.10:g.89720648_89720651dup , CM000672.1:g.89720648_89720651dup	GRCh37
NC_000010.9:g.89710628_89710631dup	NCBI36
NG_007466.2:g.102453_102456dup , LRG_311:g.102453_102456dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-3_895dup
ENST00000710265.1:c.802-3_802dup
ENST00000472832.3:c.802-3_802dup
ENST00000688158.2:n.1537-3_1537dup
ENST00000688922.2:c.*632-3_*632dup
ENST00000700021.1:c.757-3_757dup
ENST00000700022.1:c.*141-3_*141dup
ENST00000700023.1:n.1960-3_1960dup
ENST00000700024.1:n.2194-3_2194dup
ENST00000700025.1:n.1571-3_1571dup
ENST00000700026.1:n.439-3_439dup
ENST00000700029.1:c.729-3_729dup
ENST00000706954.1:c.802-3_802dup
ENST00000706955.1:c.*837-3_*837dup
ENST00000686459.1:c.*388-3_*388dup
ENST00000688158.1:c.*913-3_*913dup
ENST00000688308.1:c.802-3_802dup
ENST00000688922.1:c.723-3_723dup
ENST00000693560.1:c.1321-3_1321dup
ENST00000371953.8:c.802-3_802dup
ENST00000371953.7:c.802-3_802dup
ENST00000472832.2:c.229-3_229dup
NM_000314.5:c.802-3_802dup
NM_000314.6:c.802-3_802dup
NM_001304717.2:c.1321-3_1321dup
NM_001304718.1:c.211-3_211dup
XM_006717926.2:c.757-3_757dup
XM_011539981.1:c.802-3_802dup
XM_011539982.1:c.706-3_706dup
XR_945791.1:n.1372-3_1372dup
NM_000314.7:c.802-3_802dup
NM_001304717.5:c.1321-3_1321dup
NM_001304718.2:c.211-3_211dup
NM_000314.8:c.802-3_802dup