Canonical Allele Identifier: CA2610046383
Gene: PTEN HGNC NCBI

Linked Data

gnomAD v4: 10-87863558-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863558G>T , CM000672.2:g.87863558G>T GRCh38
NC_000010.10:g.89623315G>T , CM000672.1:g.89623315G>T GRCh37
NC_000010.9:g.89613295G>T NCBI36
NG_007466.2:g.5121G>T , LRG_311:g.5121G>T
NG_033079.1:g.4880C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-896G>T ENSP00000516674.1:n.-16-896G>T
ENST00000688308.1:c.-17+445G>T ENSP00000508752.1:n.-17+445G>T
ENST00000693560.1:c.-392G>T ENSP00000509861.1:n.-392G>T
ENST00000371953.7:c.-912G>T ENSP00000361021.3:n.-912G>T
ENST00000610634.1:c.-1014G>T ENSP00000477517.1:n.-1014G>T
NM_000314.5:c.-911G>T NP_000305.3:n.-911G>T
NM_000314.6:c.-911G>T NP_000305.3:n.-911G>T
NM_001304717.2:c.-392G>T NP_001291646.2:n.-392G>T
NM_001304718.1:c.-1616G>T NP_001291647.1:n.-1616G>T
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