Canonical Allele Identifier: CA1926143076
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863534G= , CM000672.2:g.87863534G= GRCh38
NC_000010.10:g.89623291G= , CM000672.1:g.89623291G= GRCh37
NC_000010.9:g.89613271G= NCBI36
NG_007466.2:g.5097G= , LRG_311:g.5097G=
NG_033079.1:g.4904C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+892G= ENSP00000516674.1:n.-17+892G=
ENST00000688308.1:c.-17+421G= ENSP00000508752.1:n.-17+421G=
ENST00000693560.1:c.-416G= ENSP00000509861.1:n.-416G=
ENST00000371953.7:c.-936G= ENSP00000361021.3:n.-936G=
ENST00000610634.1:c.-1038G= ENSP00000477517.1:n.-1038G=
NM_000314.5:c.-935G= NP_000305.3:n.-935G=
NM_000314.6:c.-935G= NP_000305.3:n.-935G=
NM_001304717.2:c.-416G= NP_001291646.2:n.-416G=
NM_001304718.1:c.-1640G= NP_001291647.1:n.-1640G=