Canonical Allele Identifier: CA1926143079
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863537G= , CM000672.2:g.87863537G= GRCh38
NC_000010.10:g.89623294G= , CM000672.1:g.89623294G= GRCh37
NC_000010.9:g.89613274G= NCBI36
NG_007466.2:g.5100G= , LRG_311:g.5100G=
NG_033079.1:g.4901C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+895G= ENSP00000516674.1:n.-17+895G=
ENST00000688308.1:c.-17+424G= ENSP00000508752.1:n.-17+424G=
ENST00000693560.1:c.-413G= ENSP00000509861.1:n.-413G=
ENST00000371953.7:c.-933G= ENSP00000361021.3:n.-933G=
ENST00000610634.1:c.-1035G= ENSP00000477517.1:n.-1035G=
NM_000314.5:c.-932G= NP_000305.3:n.-932G=
NM_000314.6:c.-932G= NP_000305.3:n.-932G=
NM_001304717.2:c.-413G= NP_001291646.2:n.-413G=
NM_001304718.1:c.-1637G= NP_001291647.1:n.-1637G=