Canonical Allele Identifier: CA1926143132

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863598C= , CM000672.2:g.87863598C= GRCh38
NC_000010.10:g.89623355C= , CM000672.1:g.89623355C= GRCh37
NC_000010.9:g.89613335C= NCBI36
NG_007466.2:g.5161C= , LRG_311:g.5161C=
NG_033079.1:g.4840G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-856C= (PTEN) ENSP00000516674.1:n.-16-856C=
ENST00000688308.1:c.-17+485C= (PTEN) ENSP00000508752.1:n.-17+485C=
ENST00000692337.1:c.40C= (MLDHR) ENSP00000509326.1:p.Leu14=
ENST00000693560.1:c.-352C= (PTEN) ENSP00000509861.1:n.-352C=
ENST00000371953.7:c.-872C= (PTEN) ENSP00000361021.3:n.-872C=
ENST00000610634.1:c.-974C= (PTEN) ENSP00000477517.1:n.-974C=
NM_000314.5:c.-871C= (PTEN) NP_000305.3:n.-871C=
NM_000314.6:c.-871C= (PTEN) NP_000305.3:n.-871C=
NM_001304717.2:c.-352C= (PTEN) NP_001291646.2:n.-352C=
NM_001304718.1:c.-1576C= (PTEN) NP_001291647.1:n.-1576C=