Canonical Allele Identifier: CA1926143126

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863594C= , CM000672.2:g.87863594C= GRCh38
NC_000010.10:g.89623351C= , CM000672.1:g.89623351C= GRCh37
NC_000010.9:g.89613331C= NCBI36
NG_007466.2:g.5157C= , LRG_311:g.5157C=
NG_033079.1:g.4844G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-860C= (PTEN) ENSP00000516674.1:n.-16-860C=
ENST00000688308.1:c.-17+481C= (PTEN) ENSP00000508752.1:n.-17+481C=
ENST00000692337.1:c.36C= (MLDHR) ENSP00000509326.1:p.Tyr12=
ENST00000693560.1:c.-356C= (PTEN) ENSP00000509861.1:n.-356C=
ENST00000371953.7:c.-876C= (PTEN) ENSP00000361021.3:n.-876C=
ENST00000610634.1:c.-978C= (PTEN) ENSP00000477517.1:n.-978C=
NM_000314.5:c.-875C= (PTEN) NP_000305.3:n.-875C=
NM_000314.6:c.-875C= (PTEN) NP_000305.3:n.-875C=
NM_001304717.2:c.-356C= (PTEN) NP_001291646.2:n.-356C=
NM_001304718.1:c.-1580C= (PTEN) NP_001291647.1:n.-1580C=