Canonical Allele Identifier: CA2832559829
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863526_87863535del , CM000672.2:g.87863526_87863535del GRCh38
NC_000010.10:g.89623283_89623292del , CM000672.1:g.89623283_89623292del GRCh37
NC_000010.9:g.89613263_89613272del NCBI36
NG_007466.2:g.5089_5098del , LRG_311:g.5089_5098del
NG_033079.1:g.4905_4914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+884_-17+893del ENSP00000516674.1:n.-17+884_-17+893del
ENST00000688308.1:c.-17+413_-17+422del ENSP00000508752.1:n.-17+413_-17+422del
ENST00000693560.1:c.-424_-415del ENSP00000509861.1:n.-424_-415del
ENST00000371953.7:c.-944_-935del ENSP00000361021.3:n.-944_-935del
ENST00000610634.1:c.-1046_-1037del ENSP00000477517.1:n.-1046_-1037del
NM_000314.5:c.-943_-934del NP_000305.3:n.-943_-934del
NM_000314.6:c.-943_-934del NP_000305.3:n.-943_-934del
NM_001304717.2:c.-424_-415del NP_001291646.2:n.-424_-415del
NM_001304718.1:c.-1648_-1639del NP_001291647.1:n.-1648_-1639del