Canonical Allele Identifier: CA1926143085
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863544G= , CM000672.2:g.87863544G= GRCh38
NC_000010.10:g.89623301G= , CM000672.1:g.89623301G= GRCh37
NC_000010.9:g.89613281G= NCBI36
NG_007466.2:g.5107G= , LRG_311:g.5107G=
NG_033079.1:g.4894C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+902G= ENSP00000516674.1:n.-17+902G=
ENST00000688308.1:c.-17+431G= ENSP00000508752.1:n.-17+431G=
ENST00000693560.1:c.-406G= ENSP00000509861.1:n.-406G=
ENST00000371953.7:c.-926G= ENSP00000361021.3:n.-926G=
ENST00000610634.1:c.-1028G= ENSP00000477517.1:n.-1028G=
NM_000314.5:c.-925G= NP_000305.3:n.-925G=
NM_000314.6:c.-925G= NP_000305.3:n.-925G=
NM_001304717.2:c.-406G= NP_001291646.2:n.-406G=
NM_001304718.1:c.-1630G= NP_001291647.1:n.-1630G=