Canonical Allele Identifier: CA1926143154

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863618G= , CM000672.2:g.87863618G= GRCh38
NC_000010.10:g.89623375G= , CM000672.1:g.89623375G= GRCh37
NC_000010.9:g.89613355G= NCBI36
NG_007466.2:g.5181G= , LRG_311:g.5181G=
NG_033079.1:g.4820C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-836G= (PTEN) ENSP00000516674.1:n.-16-836G=
ENST00000688308.1:c.-17+505G= (PTEN) ENSP00000508752.1:n.-17+505G=
ENST00000692337.1:c.60G= (MLDHR) ENSP00000509326.1:p.Leu20=
ENST00000693560.1:c.-332G= (PTEN) ENSP00000509861.1:n.-332G=
ENST00000371953.7:c.-852G= (PTEN) ENSP00000361021.3:n.-852G=
ENST00000610634.1:c.-954G= (PTEN) ENSP00000477517.1:n.-954G=
NM_000314.5:c.-851G= (PTEN) NP_000305.3:n.-851G=
NM_000314.6:c.-851G= (PTEN) NP_000305.3:n.-851G=
NM_001304717.2:c.-332G= (PTEN) NP_001291646.2:n.-332G=
NM_001304718.1:c.-1556G= (PTEN) NP_001291647.1:n.-1556G=