Canonical Allele Identifier: CA000609

Linked Data

ClinVar Variation Id: 127678
dbSNP Id: rs587779996

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863613C>G , CM000672.2:g.87863613C>G GRCh38
NC_000010.10:g.89623370C>G , CM000672.1:g.89623370C>G GRCh37
NC_000010.9:g.89613350C>G NCBI36
NG_007466.2:g.5176C>G , LRG_311:g.5176C>G
NG_033079.1:g.4825G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-841C>G (PTEN) ENSP00000516674.1:n.-16-841C>G
ENST00000688308.1:c.-17+500C>G (PTEN) ENSP00000508752.1:n.-17+500C>G
ENST00000692337.1:c.55C>G (MLDHR) ENSP00000509326.1:p.Arg19Gly
ENST00000693560.1:c.-337C>G (PTEN) ENSP00000509861.1:n.-337C>G
ENST00000371953.7:c.-857C>G (PTEN) ENSP00000361021.3:n.-857C>G
ENST00000610634.1:c.-959C>G (PTEN) ENSP00000477517.1:n.-959C>G
NM_000314.5:c.-856C>G (PTEN) NP_000305.3:n.-856C>G
NM_000314.6:c.-856C>G (PTEN) NP_000305.3:n.-856C>G
NM_001304717.2:c.-337C>G (PTEN) NP_001291646.2:n.-337C>G
NM_001304718.1:c.-1561C>G (PTEN) NP_001291647.1:n.-1561C>G