Canonical Allele Identifier: CA1926143215
Gene: PTEN HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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