Canonical Allele Identifier: CA1139661608

Gene: PTEN

Linked Data

• ClinVar Variation Id: 947969
• ClinVar RCV Id: RCV001219134
• dbSNP Id: rs1860608927

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960763_87961027del , CM000672.2:g.87960763_87961027del	GRCh38
NC_000010.10:g.89720520_89720784del , CM000672.1:g.89720520_89720784del	GRCh37
NC_000010.9:g.89710500_89710764del	NCBI36
NG_007466.2:g.102325_102589del , LRG_311:g.102325_102589del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-131_1028del
ENST00000710265.1:c.802-131_935del
ENST00000472832.3:c.802-131_935del
ENST00000688158.2:n.1537-131_1670del
ENST00000688922.2:c.*632-131_*765del
ENST00000700021.1:c.757-131_890del
ENST00000700022.1:c.*141-131_*274del
ENST00000700023.1:n.1960-131_2093del
ENST00000700024.1:n.2194-131_2327del
ENST00000700025.1:n.1571-131_1704del
ENST00000700026.1:n.439-131_572del
ENST00000706954.1:c.802-131_935del
ENST00000706955.1:c.*837-131_*970del
ENST00000686459.1:c.*388-131_*521del
ENST00000688158.1:c.*913-131_*1046del
ENST00000688308.1:c.802-131_935del
ENST00000688922.1:c.723-131_856del
ENST00000693560.1:c.1321-131_1454del
ENST00000371953.8:c.802-131_935del
ENST00000371953.7:c.802-131_935del
ENST00000472832.2:c.229-131_362del
NM_000314.5:c.802-131_935del
NM_000314.6:c.802-131_935del
NM_001304717.2:c.1321-131_1454del
NM_001304718.1:c.211-131_344del
XM_006717926.2:c.757-131_890del
XM_011539981.1:c.802-131_935del
XM_011539982.1:c.706-131_839del
XR_945791.1:n.1372-131_1505del
NM_000314.7:c.802-131_935del
NM_001304717.5:c.1321-131_1454del
NM_001304718.2:c.211-131_344del
NM_000314.8:c.802-131_935del