Canonical Allele Identifier: CA1926143056

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863511G= , CM000672.2:g.87863511G= GRCh38
NC_000010.10:g.89623268G= , CM000672.1:g.89623268G= GRCh37
NC_000010.9:g.89613248G= NCBI36
NG_007466.2:g.5074G= , LRG_311:g.5074G=
NG_033079.1:g.4927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+869G= (PTEN) ENSP00000516674.1:n.-17+869G=
ENST00000688308.1:c.-17+398G= (PTEN) ENSP00000508752.1:n.-17+398G=
ENST00000693560.1:c.-439G= (PTEN) ENSP00000509861.1:n.-439G=
ENST00000445946.5:c.-1024C= (KLLN) MANE Select ENSP00000392204.2:n.-1024C=
ENST00000371953.7:c.-959G= (PTEN) ENSP00000361021.3:n.-959G=
ENST00000610634.1:c.-1061G= (PTEN) ENSP00000477517.1:n.-1061G=
NM_000314.5:c.-958G= (PTEN) NP_000305.3:n.-958G=
NM_000314.6:c.-958G= (PTEN) NP_000305.3:n.-958G=
NM_001304717.2:c.-439G= (PTEN) NP_001291646.2:n.-439G=
NM_001304718.1:c.-1663G= (PTEN) NP_001291647.1:n.-1663G=
NM_001126049.2:c.-1024C= (KLLN) MANE Select NP_001119521.1:n.-1024C=