Canonical Allele Identifier: CA1926143149

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863613C= , CM000672.2:g.87863613C= GRCh38
NC_000010.10:g.89623370C= , CM000672.1:g.89623370C= GRCh37
NC_000010.9:g.89613350C= NCBI36
NG_007466.2:g.5176C= , LRG_311:g.5176C=
NG_033079.1:g.4825G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-841C= (PTEN) ENSP00000516674.1:n.-16-841C=
ENST00000688308.1:c.-17+500C= (PTEN) ENSP00000508752.1:n.-17+500C=
ENST00000692337.1:c.55C= (MLDHR) ENSP00000509326.1:p.Arg19=
ENST00000693560.1:c.-337C= (PTEN) ENSP00000509861.1:n.-337C=
ENST00000371953.7:c.-857C= (PTEN) ENSP00000361021.3:n.-857C=
ENST00000610634.1:c.-959C= (PTEN) ENSP00000477517.1:n.-959C=
NM_000314.5:c.-856C= (PTEN) NP_000305.3:n.-856C=
NM_000314.6:c.-856C= (PTEN) NP_000305.3:n.-856C=
NM_001304717.2:c.-337C= (PTEN) NP_001291646.2:n.-337C=
NM_001304718.1:c.-1561C= (PTEN) NP_001291647.1:n.-1561C=