Canonical Allele Identifier: CA1926143141

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863607G= , CM000672.2:g.87863607G= GRCh38
NC_000010.10:g.89623364G= , CM000672.1:g.89623364G= GRCh37
NC_000010.9:g.89613344G= NCBI36
NG_007466.2:g.5170G= , LRG_311:g.5170G=
NG_033079.1:g.4831C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-847G= (PTEN) ENSP00000516674.1:n.-16-847G=
ENST00000688308.1:c.-17+494G= (PTEN) ENSP00000508752.1:n.-17+494G=
ENST00000692337.1:c.49G= (MLDHR) ENSP00000509326.1:p.Gly17=
ENST00000693560.1:c.-343G= (PTEN) ENSP00000509861.1:n.-343G=
ENST00000371953.7:c.-863G= (PTEN) ENSP00000361021.3:n.-863G=
ENST00000610634.1:c.-965G= (PTEN) ENSP00000477517.1:n.-965G=
NM_000314.5:c.-862G= (PTEN) NP_000305.3:n.-862G=
NM_000314.6:c.-862G= (PTEN) NP_000305.3:n.-862G=
NM_001304717.2:c.-343G= (PTEN) NP_001291646.2:n.-343G=
NM_001304718.1:c.-1567G= (PTEN) NP_001291647.1:n.-1567G=