Canonical Allele Identifier: CA2610046391

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863578G>T , CM000672.2:g.87863578G>T GRCh38
NC_000010.10:g.89623335G>T , CM000672.1:g.89623335G>T GRCh37
NC_000010.9:g.89613315G>T NCBI36
NG_007466.2:g.5141G>T , LRG_311:g.5141G>T
NG_033079.1:g.4860C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-876G>T (PTEN) ENSP00000516674.1:n.-16-876G>T
ENST00000688308.1:c.-17+465G>T (PTEN) ENSP00000508752.1:n.-17+465G>T
ENST00000692337.1:c.20G>T (MLDHR) ENSP00000509326.1:p.Cys7Phe
ENST00000693560.1:c.-372G>T (PTEN) ENSP00000509861.1:n.-372G>T
ENST00000371953.7:c.-892G>T (PTEN) ENSP00000361021.3:n.-892G>T
ENST00000610634.1:c.-994G>T (PTEN) ENSP00000477517.1:n.-994G>T
NM_000314.5:c.-891G>T (PTEN) NP_000305.3:n.-891G>T
NM_000314.6:c.-891G>T (PTEN) NP_000305.3:n.-891G>T
NM_001304717.2:c.-372G>T (PTEN) NP_001291646.2:n.-372G>T
NM_001304718.1:c.-1596G>T (PTEN) NP_001291647.1:n.-1596G>T