Canonical Allele Identifier: CA645554135

Gene: PTEN

Linked Data

• COSMIC: COSM5752400

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961093_87961141del , CM000672.2:g.87961093_87961141del	GRCh38
NC_000010.10:g.89720850_89720898del , CM000672.1:g.89720850_89720898del	GRCh37
NC_000010.9:g.89710830_89710878del	NCBI36
NG_007466.2:g.102655_102703del , LRG_311:g.102655_102703del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1094_1119+23del
ENST00000710265.1:c.1001_1026+23del
ENST00000472832.3:c.1001_*14del	ENSP00000483066.2:n.[c.1001_*14del;Asn334...
ENST00000688158.2:n.1736_1761+23del
ENST00000688922.2:c.*831_*856+23del
ENST00000700021.1:c.956_981+23del
ENST00000700022.1:c.*340_*365+23del
ENST00000700023.1:n.2159_2184+23del
ENST00000700024.1:n.2393_2418+23del
ENST00000700025.1:n.1770_1818del
ENST00000700026.1:n.638_686del
ENST00000706954.1:c.1001_1026+23del
ENST00000706955.1:c.*1036_*1061+23del
ENST00000686459.1:c.*587_*612+23del
ENST00000688158.1:c.*1112_*1137+23del
ENST00000688308.1:c.1001_1026+23del
ENST00000688922.1:c.922_947+23del
ENST00000693560.1:c.1520_1545+23del
ENST00000371953.8:c.1001_1026+23del
ENST00000371953.7:c.1001_1026+23del
ENST00000472832.2:c.428_476del	ENSP00000483066.1:n.[c.428_476del;Asn143A...
NM_000314.5:c.1001_1026+23del
NM_000314.6:c.1001_1026+23del
NM_001304717.2:c.1520_1545+23del
NM_001304718.1:c.410_435+23del
XM_006717926.2:c.956_981+23del
XM_011539981.1:c.1001_1026+23del
XM_011539982.1:c.905_930+23del
XR_945791.1:n.1571_1596+23del
NM_000314.7:c.1001_1026+23del
NM_001304717.5:c.1520_1545+23del
NM_001304718.2:c.410_435+23del
NM_000314.8:c.1001_1026+23del