Canonical Allele Identifier: CA645558997
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132146071

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864545_87864549del , CM000672.2:g.87864545_87864549del GRCh38
NC_000010.10:g.89624302_89624306del , CM000672.1:g.89624302_89624306del GRCh37
NC_000010.9:g.89614282_89614286del NCBI36
NG_007466.2:g.6107_6111del , LRG_311:g.6107_6111del
NG_033079.1:g.3891_3895del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.76_79+1del
ENST00000710265.1:c.76_79+1del
ENST00000472832.3:c.76_79+1del
ENST00000688922.2:c.76_79+1del
ENST00000700021.1:c.76_79+1del
ENST00000700022.1:c.76_79+1del
ENST00000706954.1:c.76_79+1del
ENST00000706955.1:c.76_79+1del
ENST00000686459.1:c.76_79+1del
ENST00000688158.1:c.76_79+1del
ENST00000688308.1:c.76_79+1del
ENST00000693560.1:c.595_598+1del
ENST00000371953.8:c.76_79+1del
ENST00000371953.7:c.76_79+1del
ENST00000462694.1:n.78_81+1del
ENST00000487939.1:n.97_100+1del
ENST00000610634.1:c.-27_-24+1del
ENST00000618586.1:n.45_49del
NM_000314.5:c.76_79+1del
NM_000314.6:c.76_79+1del
NM_001304717.2:c.595_598+1del
NM_001304718.1:c.-630_-627+1del
XM_006717926.2:c.76_79+1del
XM_011539981.1:c.76_79+1del
XR_945789.1:n.788_791+1del
XR_945790.1:n.788_791+1del
XR_945791.1:n.788_791+1del
NM_000314.7:c.76_79+1del
NM_001304717.5:c.595_598+1del
NM_001304718.2:c.-630_-627+1del
NM_000314.8:c.76_79+1del