Canonical Allele Identifier: CA1926143108

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863565C= , CM000672.2:g.87863565C= GRCh38
NC_000010.10:g.89623322C= , CM000672.1:g.89623322C= GRCh37
NC_000010.9:g.89613302C= NCBI36
NG_007466.2:g.5128C= , LRG_311:g.5128C=
NG_033079.1:g.4873G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-889C= (PTEN) ENSP00000516674.1:n.-16-889C=
ENST00000688308.1:c.-17+452C= (PTEN) ENSP00000508752.1:n.-17+452C=
ENST00000692337.1:c.7C= (MLDHR) ENSP00000509326.1:p.Arg3=
ENST00000693560.1:c.-385C= (PTEN) ENSP00000509861.1:n.-385C=
ENST00000371953.7:c.-905C= (PTEN) ENSP00000361021.3:n.-905C=
ENST00000610634.1:c.-1007C= (PTEN) ENSP00000477517.1:n.-1007C=
NM_000314.5:c.-904C= (PTEN) NP_000305.3:n.-904C=
NM_000314.6:c.-904C= (PTEN) NP_000305.3:n.-904C=
NM_001304717.2:c.-385C= (PTEN) NP_001291646.2:n.-385C=
NM_001304718.1:c.-1609C= (PTEN) NP_001291647.1:n.-1609C=