Canonical Allele Identifier: CA211452760
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI

Linked Data

ClinVar Variation Id: 488764
ClinVar RCV Id: RCV000587857
dbSNP Id: rs1034838800
gnomAD v3: 10-87863611-C-G
gnomAD v4: 10-87863611-C-G
MyVariant Identifiers: chr10:g.89623368C>G (hg19) chr10:g.87863611C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863611C>G , CM000672.2:g.87863611C>G GRCh38
NC_000010.10:g.89623368C>G , CM000672.1:g.89623368C>G GRCh37
NC_000010.9:g.89613348C>G NCBI36
NG_007466.2:g.5174C>G , LRG_311:g.5174C>G
NG_033079.1:g.4827G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-843C>G (PTEN) ENSP00000516674.1:n.-16-843C>G
ENST00000688308.1:c.-17+498C>G (PTEN) ENSP00000508752.1:n.-17+498C>G
ENST00000692337.1:c.53C>G (MLDHR) ENSP00000509326.1:p.Thr18Arg
ENST00000693560.1:c.-339C>G (PTEN) ENSP00000509861.1:n.-339C>G
ENST00000371953.7:c.-859C>G (PTEN) ENSP00000361021.3:n.-859C>G
ENST00000610634.1:c.-961C>G (PTEN) ENSP00000477517.1:n.-961C>G
NM_000314.5:c.-858C>G (PTEN) NP_000305.3:n.-858C>G
NM_000314.6:c.-858C>G (PTEN) NP_000305.3:n.-858C>G
NM_001304717.2:c.-339C>G (PTEN) NP_001291646.2:n.-339C>G
NM_001304718.1:c.-1563C>G (PTEN) NP_001291647.1:n.-1563C>G
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