Canonical Allele Identifier: CA1926143210
Gene: PTEN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863691C= , CM000672.2:g.87863691C= GRCh38
NC_000010.10:g.89623448C= , CM000672.1:g.89623448C= GRCh37
NC_000010.9:g.89613428C= NCBI36
NG_007466.2:g.5254C= , LRG_311:g.5254C=
NG_033079.1:g.4747G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-779C= ENSP00000514759.2:n.-779C=
ENST00000710265.1:c.-779C= ENSP00000518161.1:n.-779C=
ENST00000706954.1:c.-16-763C= ENSP00000516674.1:n.-16-763C=
ENST00000706955.1:c.-779C= ENSP00000516675.1:n.-779C=
ENST00000688158.1:c.-779C= ENSP00000509254.1:n.-779C=
ENST00000688308.1:c.-17+578C= ENSP00000508752.1:n.-17+578C=
ENST00000693560.1:c.-259C= ENSP00000509861.1:n.-259C=
ENST00000371953.8:c.-779C= MANE Select ENSP00000361021.3:n.-779C=
ENST00000371953.7:c.-779C= ENSP00000361021.3:n.-779C=
ENST00000610634.1:c.-881C= ENSP00000477517.1:n.-881C=
NM_000314.5:c.-778C= NP_000305.3:n.-778C=
NM_000314.6:c.-778C= NP_000305.3:n.-778C=
NM_001304717.2:c.-259C= NP_001291646.2:n.-259C=
NM_001304718.1:c.-1483C= NP_001291647.1:n.-1483C=
NM_000314.7:c.-778C= NP_000305.3:n.-778C=
NM_001304717.5:c.-259C= NP_001291646.4:n.-259C=
NM_001304718.2:c.-1483C= NP_001291647.1:n.-1483C=
NM_000314.8:c.-779C= MANE Select NP_000305.3:n.-779C=
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