Canonical Allele Identifier: CA1926143161

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863624A= , CM000672.2:g.87863624A= GRCh38
NC_000010.10:g.89623381A= , CM000672.1:g.89623381A= GRCh37
NC_000010.9:g.89613361A= NCBI36
NG_007466.2:g.5187A= , LRG_311:g.5187A=
NG_033079.1:g.4814T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-830A= (PTEN) ENSP00000516674.1:n.-16-830A=
ENST00000688308.1:c.-17+511A= (PTEN) ENSP00000508752.1:n.-17+511A=
ENST00000692337.1:c.66A= (MLDHR) ENSP00000509326.1:p.Ser22=
ENST00000693560.1:c.-326A= (PTEN) ENSP00000509861.1:n.-326A=
ENST00000371953.7:c.-846A= (PTEN) ENSP00000361021.3:n.-846A=
ENST00000610634.1:c.-948A= (PTEN) ENSP00000477517.1:n.-948A=
NM_000314.5:c.-845A= (PTEN) NP_000305.3:n.-845A=
NM_000314.6:c.-845A= (PTEN) NP_000305.3:n.-845A=
NM_001304717.2:c.-326A= (PTEN) NP_001291646.2:n.-326A=
NM_001304718.1:c.-1550A= (PTEN) NP_001291647.1:n.-1550A=