Canonical Allele Identifier: CA1926143159

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863623C= , CM000672.2:g.87863623C= GRCh38
NC_000010.10:g.89623380C= , CM000672.1:g.89623380C= GRCh37
NC_000010.9:g.89613360C= NCBI36
NG_007466.2:g.5186C= , LRG_311:g.5186C=
NG_033079.1:g.4815G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-831C= (PTEN) ENSP00000516674.1:n.-16-831C=
ENST00000688308.1:c.-17+510C= (PTEN) ENSP00000508752.1:n.-17+510C=
ENST00000692337.1:c.65C= (MLDHR) ENSP00000509326.1:p.Ser22=
ENST00000693560.1:c.-327C= (PTEN) ENSP00000509861.1:n.-327C=
ENST00000371953.7:c.-847C= (PTEN) ENSP00000361021.3:n.-847C=
ENST00000610634.1:c.-949C= (PTEN) ENSP00000477517.1:n.-949C=
NM_000314.5:c.-846C= (PTEN) NP_000305.3:n.-846C=
NM_000314.6:c.-846C= (PTEN) NP_000305.3:n.-846C=
NM_001304717.2:c.-327C= (PTEN) NP_001291646.2:n.-327C=
NM_001304718.1:c.-1551C= (PTEN) NP_001291647.1:n.-1551C=