Canonical Allele Identifier: CA1926143128

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863596C= , CM000672.2:g.87863596C= GRCh38
NC_000010.10:g.89623353C= , CM000672.1:g.89623353C= GRCh37
NC_000010.9:g.89613333C= NCBI36
NG_007466.2:g.5159C= , LRG_311:g.5159C=
NG_033079.1:g.4842G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-858C= (PTEN) ENSP00000516674.1:n.-16-858C=
ENST00000688308.1:c.-17+483C= (PTEN) ENSP00000508752.1:n.-17+483C=
ENST00000692337.1:c.38C= (MLDHR) ENSP00000509326.1:p.Ala13=
ENST00000693560.1:c.-354C= (PTEN) ENSP00000509861.1:n.-354C=
ENST00000371953.7:c.-874C= (PTEN) ENSP00000361021.3:n.-874C=
ENST00000610634.1:c.-976C= (PTEN) ENSP00000477517.1:n.-976C=
NM_000314.5:c.-873C= (PTEN) NP_000305.3:n.-873C=
NM_000314.6:c.-873C= (PTEN) NP_000305.3:n.-873C=
NM_001304717.2:c.-354C= (PTEN) NP_001291646.2:n.-354C=
NM_001304718.1:c.-1578C= (PTEN) NP_001291647.1:n.-1578C=