Canonical Allele Identifier: CA1926143160

Linked Data

dbSNP Id: rs786204860

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863623C>G , CM000672.2:g.87863623C>G GRCh38
NC_000010.10:g.89623380C>G , CM000672.1:g.89623380C>G GRCh37
NC_000010.9:g.89613360C>G NCBI36
NG_007466.2:g.5186C>G , LRG_311:g.5186C>G
NG_033079.1:g.4815G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-831C>G (PTEN) ENSP00000516674.1:n.-16-831C>G
ENST00000688308.1:c.-17+510C>G (PTEN) ENSP00000508752.1:n.-17+510C>G
ENST00000692337.1:c.65C>G (MLDHR) ENSP00000509326.1:p.Ser22Ter
ENST00000693560.1:c.-327C>G (PTEN) ENSP00000509861.1:n.-327C>G
ENST00000371953.7:c.-847C>G (PTEN) ENSP00000361021.3:n.-847C>G
ENST00000610634.1:c.-949C>G (PTEN) ENSP00000477517.1:n.-949C>G
NM_000314.5:c.-846C>G (PTEN) NP_000305.3:n.-846C>G
NM_000314.6:c.-846C>G (PTEN) NP_000305.3:n.-846C>G
NM_001304717.2:c.-327C>G (PTEN) NP_001291646.2:n.-327C>G
NM_001304718.1:c.-1551C>G (PTEN) NP_001291647.1:n.-1551C>G