Canonical Allele Identifier: CA2610046400

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863593A>G , CM000672.2:g.87863593A>G GRCh38
NC_000010.10:g.89623350A>G , CM000672.1:g.89623350A>G GRCh37
NC_000010.9:g.89613330A>G NCBI36
NG_007466.2:g.5156A>G , LRG_311:g.5156A>G
NG_033079.1:g.4845T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-861A>G (PTEN) ENSP00000516674.1:n.-16-861A>G
ENST00000688308.1:c.-17+480A>G (PTEN) ENSP00000508752.1:n.-17+480A>G
ENST00000692337.1:c.35A>G (MLDHR) ENSP00000509326.1:p.Tyr12Cys
ENST00000693560.1:c.-357A>G (PTEN) ENSP00000509861.1:n.-357A>G
ENST00000371953.7:c.-877A>G (PTEN) ENSP00000361021.3:n.-877A>G
ENST00000610634.1:c.-979A>G (PTEN) ENSP00000477517.1:n.-979A>G
NM_000314.5:c.-876A>G (PTEN) NP_000305.3:n.-876A>G
NM_000314.6:c.-876A>G (PTEN) NP_000305.3:n.-876A>G
NM_001304717.2:c.-357A>G (PTEN) NP_001291646.2:n.-357A>G
NM_001304718.1:c.-1581A>G (PTEN) NP_001291647.1:n.-1581A>G