Canonical Allele Identifier: CA2610046380
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863554del , CM000672.2:g.87863554del GRCh38
NC_000010.10:g.89623311del , CM000672.1:g.89623311del GRCh37
NC_000010.9:g.89613291del NCBI36
NG_007466.2:g.5117del , LRG_311:g.5117del
NG_033079.1:g.4884del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-900del ENSP00000516674.1:n.-16-900del
ENST00000688308.1:c.-17+441del ENSP00000508752.1:n.-17+441del
ENST00000693560.1:c.-396del ENSP00000509861.1:n.-396del
ENST00000371953.7:c.-916del ENSP00000361021.3:n.-916del
ENST00000610634.1:c.-1018del ENSP00000477517.1:n.-1018del
NM_000314.5:c.-915del NP_000305.3:n.-915del
NM_000314.6:c.-915del NP_000305.3:n.-915del
NM_001304717.2:c.-396del NP_001291646.2:n.-396del
NM_001304718.1:c.-1620del NP_001291647.1:n.-1620del