Canonical Allele Identifier: CA2610046388

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863569A>G , CM000672.2:g.87863569A>G GRCh38
NC_000010.10:g.89623326A>G , CM000672.1:g.89623326A>G GRCh37
NC_000010.9:g.89613306A>G NCBI36
NG_007466.2:g.5132A>G , LRG_311:g.5132A>G
NG_033079.1:g.4869T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-885A>G (PTEN) ENSP00000516674.1:n.-16-885A>G
ENST00000688308.1:c.-17+456A>G (PTEN) ENSP00000508752.1:n.-17+456A>G
ENST00000692337.1:c.11A>G (MLDHR) ENSP00000509326.1:p.Asp4Gly
ENST00000693560.1:c.-381A>G (PTEN) ENSP00000509861.1:n.-381A>G
ENST00000371953.7:c.-901A>G (PTEN) ENSP00000361021.3:n.-901A>G
ENST00000610634.1:c.-1003A>G (PTEN) ENSP00000477517.1:n.-1003A>G
NM_000314.5:c.-900A>G (PTEN) NP_000305.3:n.-900A>G
NM_000314.6:c.-900A>G (PTEN) NP_000305.3:n.-900A>G
NM_001304717.2:c.-381A>G (PTEN) NP_001291646.2:n.-381A>G
NM_001304718.1:c.-1605A>G (PTEN) NP_001291647.1:n.-1605A>G