Canonical Allele Identifier: CA1926143083
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863542C= , CM000672.2:g.87863542C= GRCh38
NC_000010.10:g.89623299C= , CM000672.1:g.89623299C= GRCh37
NC_000010.9:g.89613279C= NCBI36
NG_007466.2:g.5105C= , LRG_311:g.5105C=
NG_033079.1:g.4896G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+900C= ENSP00000516674.1:n.-17+900C=
ENST00000688308.1:c.-17+429C= ENSP00000508752.1:n.-17+429C=
ENST00000693560.1:c.-408C= ENSP00000509861.1:n.-408C=
ENST00000371953.7:c.-928C= ENSP00000361021.3:n.-928C=
ENST00000610634.1:c.-1030C= ENSP00000477517.1:n.-1030C=
NM_000314.5:c.-927C= NP_000305.3:n.-927C=
NM_000314.6:c.-927C= NP_000305.3:n.-927C=
NM_001304717.2:c.-408C= NP_001291646.2:n.-408C=
NM_001304718.1:c.-1632C= NP_001291647.1:n.-1632C=