Canonical Allele Identifier: CA645554127

Gene: PTEN

Linked Data

• COSMIC: COSM5795

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961069_87961123del , CM000672.2:g.87961069_87961123del	GRCh38
NC_000010.10:g.89720826_89720880del , CM000672.1:g.89720826_89720880del	GRCh37
NC_000010.9:g.89710806_89710860del	NCBI36
NG_007466.2:g.102631_102685del , LRG_311:g.102631_102685del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1070_1119+5del
ENST00000710265.1:c.977_1026+5del
ENST00000472832.3:c.977_1031del	ENSP00000483066.2:p.Asp326ValfsTer19
ENST00000688158.2:n.1712_1761+5del
ENST00000688922.2:c.*807_*856+5del
ENST00000700021.1:c.932_981+5del
ENST00000700022.1:c.*316_*365+5del
ENST00000700023.1:n.2135_2184+5del
ENST00000700024.1:n.2369_2418+5del
ENST00000700025.1:n.1746_1800del
ENST00000700026.1:n.614_668del
ENST00000706954.1:c.977_1026+5del
ENST00000706955.1:c.*1012_*1061+5del
ENST00000686459.1:c.*563_*612+5del
ENST00000688158.1:c.*1088_*1137+5del
ENST00000688308.1:c.977_1026+5del
ENST00000688922.1:c.898_947+5del
ENST00000693560.1:c.1496_1545+5del
ENST00000371953.8:c.977_1026+5del
ENST00000371953.7:c.977_1026+5del
ENST00000472832.2:c.404_458del	ENSP00000483066.1:p.Asp135ValfsTer19
NM_000314.5:c.977_1026+5del
NM_000314.6:c.977_1026+5del
NM_001304717.2:c.1496_1545+5del
NM_001304718.1:c.386_435+5del
XM_006717926.2:c.932_981+5del
XM_011539981.1:c.977_1026+5del
XM_011539982.1:c.881_930+5del
XR_945791.1:n.1547_1596+5del
NM_000314.7:c.977_1026+5del
NM_001304717.5:c.1496_1545+5del
NM_001304718.2:c.386_435+5del
NM_000314.8:c.977_1026+5del