Canonical Allele Identifier: CA1926143195
Gene: PTEN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863664G= , CM000672.2:g.87863664G= GRCh38
NC_000010.10:g.89623421G= , CM000672.1:g.89623421G= GRCh37
NC_000010.9:g.89613401G= NCBI36
NG_007466.2:g.5227G= , LRG_311:g.5227G=
NG_033079.1:g.4774C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-806G= ENSP00000514759.2:n.-806G=
ENST00000710265.1:c.-806G= ENSP00000518161.1:n.-806G=
ENST00000706954.1:c.-16-790G= ENSP00000516674.1:n.-16-790G=
ENST00000706955.1:c.-806G= ENSP00000516675.1:n.-806G=
ENST00000688158.1:c.-806G= ENSP00000509254.1:n.-806G=
ENST00000688308.1:c.-17+551G= ENSP00000508752.1:n.-17+551G=
ENST00000693560.1:c.-286G= ENSP00000509861.1:n.-286G=
ENST00000371953.8:c.-806G= MANE Select ENSP00000361021.3:n.-806G=
ENST00000371953.7:c.-806G= ENSP00000361021.3:n.-806G=
ENST00000610634.1:c.-908G= ENSP00000477517.1:n.-908G=
NM_000314.5:c.-805G= NP_000305.3:n.-805G=
NM_000314.6:c.-805G= NP_000305.3:n.-805G=
NM_001304717.2:c.-286G= NP_001291646.2:n.-286G=
NM_001304718.1:c.-1510G= NP_001291647.1:n.-1510G=
NM_000314.7:c.-805G= NP_000305.3:n.-805G=
NM_001304717.5:c.-286G= NP_001291646.4:n.-286G=
NM_001304718.2:c.-1510G= NP_001291647.1:n.-1510G=
NM_000314.8:c.-806G= MANE Select NP_000305.3:n.-806G=
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