Canonical Allele Identifier: CA16612913
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 404158
ClinVar RCV Id: RCV000462895
dbSNP Id: rs1064792911

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960890_87960896delinsA , CM000672.2:g.87960890_87960896delinsA GRCh38
NC_000010.10:g.89720647_89720653delinsA , CM000672.1:g.89720647_89720653delinsA GRCh37
NC_000010.9:g.89710627_89710633delinsA NCBI36
NG_007466.2:g.102452_102458delinsA , LRG_311:g.102452_102458delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-4_897delinsA
ENST00000710265.1:c.802-4_804delinsA
ENST00000472832.3:c.802-4_804delinsA
ENST00000688158.2:n.1537-4_1539delinsA
ENST00000688922.2:c.*632-4_*634delinsA
ENST00000700021.1:c.757-4_759delinsA
ENST00000700022.1:c.*141-4_*143delinsA
ENST00000700023.1:n.1960-4_1962delinsA
ENST00000700024.1:n.2194-4_2196delinsA
ENST00000700025.1:n.1571-4_1573delinsA
ENST00000700026.1:n.439-4_441delinsA
ENST00000700029.1:c.729-4_731delinsA
ENST00000706954.1:c.802-4_804delinsA
ENST00000706955.1:c.*837-4_*839delinsA
ENST00000686459.1:c.*388-4_*390delinsA
ENST00000688158.1:c.*913-4_*915delinsA
ENST00000688308.1:c.802-4_804delinsA
ENST00000688922.1:c.723-4_725delinsA
ENST00000693560.1:c.1321-4_1323delinsA
ENST00000371953.8:c.802-4_804delinsA
ENST00000371953.7:c.802-4_804delinsA
ENST00000472832.2:c.229-4_231delinsA
NM_000314.5:c.802-4_804delinsA
NM_000314.6:c.802-4_804delinsA
NM_001304717.2:c.1321-4_1323delinsA
NM_001304718.1:c.211-4_213delinsA
XM_006717926.2:c.757-4_759delinsA
XM_011539981.1:c.802-4_804delinsA
XM_011539982.1:c.706-4_708delinsA
XR_945791.1:n.1372-4_1374delinsA
NM_000314.7:c.802-4_804delinsA
NM_001304717.5:c.1321-4_1323delinsA
NM_001304718.2:c.211-4_213delinsA
NM_000314.8:c.802-4_804delinsA