Canonical Allele Identifier: CA2610046420

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863636T>C , CM000672.2:g.87863636T>C GRCh38
NC_000010.10:g.89623393T>C , CM000672.1:g.89623393T>C GRCh37
NC_000010.9:g.89613373T>C NCBI36
NG_007466.2:g.5199T>C , LRG_311:g.5199T>C
NG_033079.1:g.4802A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-834T>C (PTEN) ENSP00000514759.2:n.-834T>C
ENST00000710265.1:c.-834T>C (PTEN) ENSP00000518161.1:n.-834T>C
ENST00000706954.1:c.-16-818T>C (PTEN) ENSP00000516674.1:n.-16-818T>C
ENST00000706955.1:c.-834T>C (PTEN) ENSP00000516675.1:n.-834T>C
ENST00000688158.1:c.-834T>C (PTEN) ENSP00000509254.1:n.-834T>C
ENST00000688308.1:c.-17+523T>C (PTEN) ENSP00000508752.1:n.-17+523T>C
ENST00000692337.1:c.78T>C (MLDHR) ENSP00000509326.1:p.Ser26=
ENST00000693560.1:c.-314T>C (PTEN) ENSP00000509861.1:n.-314T>C
ENST00000371953.8:c.-834T>C (PTEN) MANE Select ENSP00000361021.3:n.-834T>C
ENST00000371953.7:c.-834T>C (PTEN) ENSP00000361021.3:n.-834T>C
ENST00000610634.1:c.-936T>C (PTEN) ENSP00000477517.1:n.-936T>C
NM_000314.5:c.-833T>C (PTEN) NP_000305.3:n.-833T>C
NM_000314.6:c.-833T>C (PTEN) NP_000305.3:n.-833T>C
NM_001304717.2:c.-314T>C (PTEN) NP_001291646.2:n.-314T>C
NM_001304718.1:c.-1538T>C (PTEN) NP_001291647.1:n.-1538T>C
NM_000314.7:c.-833T>C (PTEN) NP_000305.3:n.-833T>C
NM_001304717.5:c.-314T>C (PTEN) NP_001291646.4:n.-314T>C
NM_001304718.2:c.-1538T>C (PTEN) NP_001291647.1:n.-1538T>C
NM_000314.8:c.-834T>C (PTEN) MANE Select NP_000305.3:n.-834T>C