Canonical Allele Identifier: CA2610046463
Gene: PTEN HGNC NCBI

Linked Data

gnomAD v4: 10-87863698-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863698A>T , CM000672.2:g.87863698A>T GRCh38
NC_000010.10:g.89623455A>T , CM000672.1:g.89623455A>T GRCh37
NC_000010.9:g.89613435A>T NCBI36
NG_007466.2:g.5261A>T , LRG_311:g.5261A>T
NG_033079.1:g.4740T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-772A>T ENSP00000514759.2:n.-772A>T
ENST00000710265.1:c.-772A>T ENSP00000518161.1:n.-772A>T
ENST00000706954.1:c.-16-756A>T ENSP00000516674.1:n.-16-756A>T
ENST00000706955.1:c.-772A>T ENSP00000516675.1:n.-772A>T
ENST00000688158.1:c.-772A>T ENSP00000509254.1:n.-772A>T
ENST00000688308.1:c.-17+585A>T ENSP00000508752.1:n.-17+585A>T
ENST00000693560.1:c.-252A>T ENSP00000509861.1:n.-252A>T
ENST00000371953.8:c.-772A>T MANE Select ENSP00000361021.3:n.-772A>T
ENST00000371953.7:c.-772A>T ENSP00000361021.3:n.-772A>T
ENST00000610634.1:c.-874A>T ENSP00000477517.1:n.-874A>T
NM_000314.5:c.-771A>T NP_000305.3:n.-771A>T
NM_000314.6:c.-771A>T NP_000305.3:n.-771A>T
NM_001304717.2:c.-252A>T NP_001291646.2:n.-252A>T
NM_001304718.1:c.-1476A>T NP_001291647.1:n.-1476A>T
NM_000314.7:c.-771A>T NP_000305.3:n.-771A>T
NM_001304717.5:c.-252A>T NP_001291646.4:n.-252A>T
NM_001304718.2:c.-1476A>T NP_001291647.1:n.-1476A>T
NM_000314.8:c.-772A>T MANE Select NP_000305.3:n.-772A>T
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