Canonical Allele Identifier: CA2610046401
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2663044
ClinVar RCV Id: RCV003442232
gnomAD v4: 10-87863594-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863594C>T , CM000672.2:g.87863594C>T GRCh38
NC_000010.10:g.89623351C>T , CM000672.1:g.89623351C>T GRCh37
NC_000010.9:g.89613331C>T NCBI36
NG_007466.2:g.5157C>T , LRG_311:g.5157C>T
NG_033079.1:g.4844G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-860C>T (PTEN) ENSP00000516674.1:n.-16-860C>T
ENST00000688308.1:c.-17+481C>T (PTEN) ENSP00000508752.1:n.-17+481C>T
ENST00000692337.1:c.36C>T (MLDHR) ENSP00000509326.1:p.Tyr12=
ENST00000693560.1:c.-356C>T (PTEN) ENSP00000509861.1:n.-356C>T
ENST00000371953.7:c.-876C>T (PTEN) ENSP00000361021.3:n.-876C>T
ENST00000610634.1:c.-978C>T (PTEN) ENSP00000477517.1:n.-978C>T
NM_000314.5:c.-875C>T (PTEN) NP_000305.3:n.-875C>T
NM_000314.6:c.-875C>T (PTEN) NP_000305.3:n.-875C>T
NM_001304717.2:c.-356C>T (PTEN) NP_001291646.2:n.-356C>T
NM_001304718.1:c.-1580C>T (PTEN) NP_001291647.1:n.-1580C>T
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