Canonical Allele Identifier: CA1926143117

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863576A= , CM000672.2:g.87863576A= GRCh38
NC_000010.10:g.89623333A= , CM000672.1:g.89623333A= GRCh37
NC_000010.9:g.89613313A= NCBI36
NG_007466.2:g.5139A= , LRG_311:g.5139A=
NG_033079.1:g.4862T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-878A= (PTEN) ENSP00000516674.1:n.-16-878A=
ENST00000688308.1:c.-17+463A= (PTEN) ENSP00000508752.1:n.-17+463A=
ENST00000692337.1:c.18A= (MLDHR) ENSP00000509326.1:p.Leu6=
ENST00000693560.1:c.-374A= (PTEN) ENSP00000509861.1:n.-374A=
ENST00000371953.7:c.-894A= (PTEN) ENSP00000361021.3:n.-894A=
ENST00000610634.1:c.-996A= (PTEN) ENSP00000477517.1:n.-996A=
NM_000314.5:c.-893A= (PTEN) NP_000305.3:n.-893A=
NM_000314.6:c.-893A= (PTEN) NP_000305.3:n.-893A=
NM_001304717.2:c.-374A= (PTEN) NP_001291646.2:n.-374A=
NM_001304718.1:c.-1598A= (PTEN) NP_001291647.1:n.-1598A=