Canonical Allele Identifier: CA1926143091
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863547C= , CM000672.2:g.87863547C= GRCh38
NC_000010.10:g.89623304C= , CM000672.1:g.89623304C= GRCh37
NC_000010.9:g.89613284C= NCBI36
NG_007466.2:g.5110C= , LRG_311:g.5110C=
NG_033079.1:g.4891G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+905C= ENSP00000516674.1:n.-17+905C=
ENST00000688308.1:c.-17+434C= ENSP00000508752.1:n.-17+434C=
ENST00000693560.1:c.-403C= ENSP00000509861.1:n.-403C=
ENST00000371953.7:c.-923C= ENSP00000361021.3:n.-923C=
ENST00000610634.1:c.-1025C= ENSP00000477517.1:n.-1025C=
NM_000314.5:c.-922C= NP_000305.3:n.-922C=
NM_000314.6:c.-922C= NP_000305.3:n.-922C=
NM_001304717.2:c.-403C= NP_001291646.2:n.-403C=
NM_001304718.1:c.-1627C= NP_001291647.1:n.-1627C=