Canonical Allele Identifier: CA1926143096
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863553G= , CM000672.2:g.87863553G= GRCh38
NC_000010.10:g.89623310G= , CM000672.1:g.89623310G= GRCh37
NC_000010.9:g.89613290G= NCBI36
NG_007466.2:g.5116G= , LRG_311:g.5116G=
NG_033079.1:g.4885C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-901G= ENSP00000516674.1:n.-16-901G=
ENST00000688308.1:c.-17+440G= ENSP00000508752.1:n.-17+440G=
ENST00000693560.1:c.-397G= ENSP00000509861.1:n.-397G=
ENST00000371953.7:c.-917G= ENSP00000361021.3:n.-917G=
ENST00000610634.1:c.-1019G= ENSP00000477517.1:n.-1019G=
NM_000314.5:c.-916G= NP_000305.3:n.-916G=
NM_000314.6:c.-916G= NP_000305.3:n.-916G=
NM_001304717.2:c.-397G= NP_001291646.2:n.-397G=
NM_001304718.1:c.-1621G= NP_001291647.1:n.-1621G=