Canonical Allele Identifier: CA653764295

Gene: PTEN

Linked Data

• COSMIC: COSN20083004 ; COSN20083008 ; COSN20083011 ; COSN20083014 ; COSN20083018 ; COSN20083022 ; COSN20083025 ; COSN20083028

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966989dup , CM000672.2:g.87966989dup	GRCh38
NC_000010.10:g.89726746dup , CM000672.1:g.89726746dup	GRCh37
NC_000010.9:g.89716726dup	NCBI36
NG_007466.2:g.108551dup , LRG_311:g.108551dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000710265.1:c.*1758dup	ENSP00000518161.1:n.*1758dup
ENST00000688158.2:n.3464dup
ENST00000706954.1:c.*1517dup	ENSP00000516674.1:n.*1517dup
ENST00000706955.1:c.*2764dup	ENSP00000516675.1:n.*2764dup
ENST00000688158.1:c.*2840dup	ENSP00000509254.1:n.*2840dup
ENST00000693560.1:c.*1517dup	ENSP00000509861.1:n.*1517dup
ENST00000371953.8:c.*1517dup MANE Select	ENSP00000361021.3:n.*1517dup
ENST00000371953.7:c.*1517dup	ENSP00000361021.3:n.*1517dup
NM_000314.5:c.*1517dup	NP_000305.3:n.*1517dup
NM_000314.6:c.*1517dup	NP_000305.3:n.*1517dup
NM_001304717.2:c.*1517dup	NP_001291646.2:n.*1517dup
NM_001304718.1:c.*1517dup	NP_001291647.1:n.*1517dup
XM_006717926.2:c.*1517dup	XP_006717989.1:n.*1517dup
XM_011539982.1:c.*1517dup	XP_011538284.1:n.*1517dup
XR_945791.1:n.3299dup
NM_000314.7:c.*1517dup	NP_000305.3:n.*1517dup
NM_001304717.5:c.*1517dup	NP_001291646.4:n.*1517dup
NM_001304718.2:c.*1517dup	NP_001291647.1:n.*1517dup
NM_000314.8:c.*1517dup MANE Select	NP_000305.3:n.*1517dup