Canonical Allele Identifier: CA1926143111
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863567G= , CM000672.2:g.87863567G= GRCh38
NC_000010.10:g.89623324G= , CM000672.1:g.89623324G= GRCh37
NC_000010.9:g.89613304G= NCBI36
NG_007466.2:g.5130G= , LRG_311:g.5130G=
NG_033079.1:g.4871C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-887G= (PTEN) ENSP00000516674.1:n.-16-887G=
ENST00000688308.1:c.-17+454G= (PTEN) ENSP00000508752.1:n.-17+454G=
ENST00000692337.1:c.9G= (MLDHR) ENSP00000509326.1:p.Arg3=
ENST00000693560.1:c.-383G= (PTEN) ENSP00000509861.1:n.-383G=
ENST00000371953.7:c.-903G= (PTEN) ENSP00000361021.3:n.-903G=
ENST00000610634.1:c.-1005G= (PTEN) ENSP00000477517.1:n.-1005G=
NM_000314.5:c.-902G= (PTEN) NP_000305.3:n.-902G=
NM_000314.6:c.-902G= (PTEN) NP_000305.3:n.-902G=
NM_001304717.2:c.-383G= (PTEN) NP_001291646.2:n.-383G=
NM_001304718.1:c.-1607G= (PTEN) NP_001291647.1:n.-1607G=
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