Canonical Allele Identifier: CA2580082286

Gene: PTEN

Linked Data

• ClinVar Variation Id: 2027181
• ClinVar RCV Id: RCV002866493 ; RCV003455588

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957821_87957861del , CM000672.2:g.87957821_87957861del	GRCh38
NC_000010.10:g.89717578_89717618del , CM000672.1:g.89717578_89717618del	GRCh37
NC_000010.9:g.89707558_89707598del	NCBI36
NG_007466.2:g.99383_99423del , LRG_311:g.99383_99423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635-32_643del
ENST00000710265.1:c.635-32_643del
ENST00000472832.3:c.635-32_643del
ENST00000688158.2:n.1370-32_1378del
ENST00000688922.2:c.*465-32_*473del
ENST00000700021.1:c.590-32_598del
ENST00000700022.1:c.493-32_501del
ENST00000700023.1:n.1793-32_1801del
ENST00000700024.1:n.2027-32_2035del
ENST00000700025.1:n.1404-32_1412del
ENST00000700026.1:n.240_280del
ENST00000700029.1:c.469-32_477del
ENST00000706954.1:c.635-32_643del
ENST00000706955.1:c.*670-32_*678del
ENST00000686459.1:c.*221-32_*229del
ENST00000688158.1:c.*746-32_*754del
ENST00000688308.1:c.635-32_643del
ENST00000688922.1:c.556-32_564del
ENST00000693560.1:c.1154-32_1162del
ENST00000371953.8:c.635-32_643del
ENST00000371953.7:c.635-32_643del
ENST00000472832.2:c.62-32_70del
NM_000314.5:c.635-32_643del
NM_000314.6:c.635-32_643del
NM_001304717.2:c.1154-32_1162del
NM_001304718.1:c.44-32_52del
XM_006717926.2:c.590-32_598del
XM_011539981.1:c.635-32_643del
XM_011539982.1:c.539-32_547del
XR_945791.1:n.1205-32_1213del
NM_000314.7:c.635-32_643del
NM_001304717.5:c.1154-32_1162del
NM_001304718.2:c.44-32_52del
NM_000314.8:c.635-32_643del