Canonical Allele Identifier: CA1926143205
Gene: PTEN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863679G= , CM000672.2:g.87863679G= GRCh38
NC_000010.10:g.89623436G= , CM000672.1:g.89623436G= GRCh37
NC_000010.9:g.89613416G= NCBI36
NG_007466.2:g.5242G= , LRG_311:g.5242G=
NG_033079.1:g.4759C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-791G= ENSP00000514759.2:n.-791G=
ENST00000710265.1:c.-791G= ENSP00000518161.1:n.-791G=
ENST00000706954.1:c.-16-775G= ENSP00000516674.1:n.-16-775G=
ENST00000706955.1:c.-791G= ENSP00000516675.1:n.-791G=
ENST00000688158.1:c.-791G= ENSP00000509254.1:n.-791G=
ENST00000688308.1:c.-17+566G= ENSP00000508752.1:n.-17+566G=
ENST00000693560.1:c.-271G= ENSP00000509861.1:n.-271G=
ENST00000371953.8:c.-791G= MANE Select ENSP00000361021.3:n.-791G=
ENST00000371953.7:c.-791G= ENSP00000361021.3:n.-791G=
ENST00000610634.1:c.-893G= ENSP00000477517.1:n.-893G=
NM_000314.5:c.-790G= NP_000305.3:n.-790G=
NM_000314.6:c.-790G= NP_000305.3:n.-790G=
NM_001304717.2:c.-271G= NP_001291646.2:n.-271G=
NM_001304718.1:c.-1495G= NP_001291647.1:n.-1495G=
NM_000314.7:c.-790G= NP_000305.3:n.-790G=
NM_001304717.5:c.-271G= NP_001291646.4:n.-271G=
NM_001304718.2:c.-1495G= NP_001291647.1:n.-1495G=
NM_000314.8:c.-791G= MANE Select NP_000305.3:n.-791G=
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