Canonical Allele Identifier: CA1926143146

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863611C= , CM000672.2:g.87863611C= GRCh38
NC_000010.10:g.89623368C= , CM000672.1:g.89623368C= GRCh37
NC_000010.9:g.89613348C= NCBI36
NG_007466.2:g.5174C= , LRG_311:g.5174C=
NG_033079.1:g.4827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-843C= (PTEN) ENSP00000516674.1:n.-16-843C=
ENST00000688308.1:c.-17+498C= (PTEN) ENSP00000508752.1:n.-17+498C=
ENST00000692337.1:c.53C= (MLDHR) ENSP00000509326.1:p.Thr18=
ENST00000693560.1:c.-339C= (PTEN) ENSP00000509861.1:n.-339C=
ENST00000371953.7:c.-859C= (PTEN) ENSP00000361021.3:n.-859C=
ENST00000610634.1:c.-961C= (PTEN) ENSP00000477517.1:n.-961C=
NM_000314.5:c.-858C= (PTEN) NP_000305.3:n.-858C=
NM_000314.6:c.-858C= (PTEN) NP_000305.3:n.-858C=
NM_001304717.2:c.-339C= (PTEN) NP_001291646.2:n.-339C=
NM_001304718.1:c.-1563C= (PTEN) NP_001291647.1:n.-1563C=