Canonical Allele Identifier: CA1926143150

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863614G= , CM000672.2:g.87863614G= GRCh38
NC_000010.10:g.89623371G= , CM000672.1:g.89623371G= GRCh37
NC_000010.9:g.89613351G= NCBI36
NG_007466.2:g.5177G= , LRG_311:g.5177G=
NG_033079.1:g.4824C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-840G= (PTEN) ENSP00000516674.1:n.-16-840G=
ENST00000688308.1:c.-17+501G= (PTEN) ENSP00000508752.1:n.-17+501G=
ENST00000692337.1:c.56G= (MLDHR) ENSP00000509326.1:p.Arg19=
ENST00000693560.1:c.-336G= (PTEN) ENSP00000509861.1:n.-336G=
ENST00000371953.7:c.-856G= (PTEN) ENSP00000361021.3:n.-856G=
ENST00000610634.1:c.-958G= (PTEN) ENSP00000477517.1:n.-958G=
NM_000314.5:c.-855G= (PTEN) NP_000305.3:n.-855G=
NM_000314.6:c.-855G= (PTEN) NP_000305.3:n.-855G=
NM_001304717.2:c.-336G= (PTEN) NP_001291646.2:n.-336G=
NM_001304718.1:c.-1560G= (PTEN) NP_001291647.1:n.-1560G=