Canonical Allele Identifier: CA1926143212
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863692G= , CM000672.2:g.87863692G= GRCh38
NC_000010.10:g.89623449G= , CM000672.1:g.89623449G= GRCh37
NC_000010.9:g.89613429G= NCBI36
NG_007466.2:g.5255G= , LRG_311:g.5255G=
NG_033079.1:g.4746C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-778G= ENSP00000514759.2:n.-778G=
ENST00000710265.1:c.-778G= ENSP00000518161.1:n.-778G=
ENST00000706954.1:c.-16-762G= ENSP00000516674.1:n.-16-762G=
ENST00000706955.1:c.-778G= ENSP00000516675.1:n.-778G=
ENST00000688158.1:c.-778G= ENSP00000509254.1:n.-778G=
ENST00000688308.1:c.-17+579G= ENSP00000508752.1:n.-17+579G=
ENST00000693560.1:c.-258G= ENSP00000509861.1:n.-258G=
ENST00000371953.8:c.-778G= MANE Select ENSP00000361021.3:n.-778G=
ENST00000371953.7:c.-778G= ENSP00000361021.3:n.-778G=
ENST00000610634.1:c.-880G= ENSP00000477517.1:n.-880G=
NM_000314.5:c.-777G= NP_000305.3:n.-777G=
NM_000314.6:c.-777G= NP_000305.3:n.-777G=
NM_001304717.2:c.-258G= NP_001291646.2:n.-258G=
NM_001304718.1:c.-1482G= NP_001291647.1:n.-1482G=
NM_000314.7:c.-777G= NP_000305.3:n.-777G=
NM_001304717.5:c.-258G= NP_001291646.4:n.-258G=
NM_001304718.2:c.-1482G= NP_001291647.1:n.-1482G=
NM_000314.8:c.-778G= MANE Select NP_000305.3:n.-778G=