Canonical Allele Identifier: CA1926143152

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863615A= , CM000672.2:g.87863615A= GRCh38
NC_000010.10:g.89623372A= , CM000672.1:g.89623372A= GRCh37
NC_000010.9:g.89613352A= NCBI36
NG_007466.2:g.5178A= , LRG_311:g.5178A=
NG_033079.1:g.4823T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-839A= (PTEN) ENSP00000516674.1:n.-16-839A=
ENST00000688308.1:c.-17+502A= (PTEN) ENSP00000508752.1:n.-17+502A=
ENST00000692337.1:c.57A= (MLDHR) ENSP00000509326.1:p.Arg19=
ENST00000693560.1:c.-335A= (PTEN) ENSP00000509861.1:n.-335A=
ENST00000371953.7:c.-855A= (PTEN) ENSP00000361021.3:n.-855A=
ENST00000610634.1:c.-957A= (PTEN) ENSP00000477517.1:n.-957A=
NM_000314.5:c.-854A= (PTEN) NP_000305.3:n.-854A=
NM_000314.6:c.-854A= (PTEN) NP_000305.3:n.-854A=
NM_001304717.2:c.-335A= (PTEN) NP_001291646.2:n.-335A=
NM_001304718.1:c.-1559A= (PTEN) NP_001291647.1:n.-1559A=