Canonical Allele Identifier: CA1926143094
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863551G= , CM000672.2:g.87863551G= GRCh38
NC_000010.10:g.89623308G= , CM000672.1:g.89623308G= GRCh37
NC_000010.9:g.89613288G= NCBI36
NG_007466.2:g.5114G= , LRG_311:g.5114G=
NG_033079.1:g.4887C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-903G= ENSP00000516674.1:n.-16-903G=
ENST00000688308.1:c.-17+438G= ENSP00000508752.1:n.-17+438G=
ENST00000693560.1:c.-399G= ENSP00000509861.1:n.-399G=
ENST00000371953.7:c.-919G= ENSP00000361021.3:n.-919G=
ENST00000610634.1:c.-1021G= ENSP00000477517.1:n.-1021G=
NM_000314.5:c.-918G= NP_000305.3:n.-918G=
NM_000314.6:c.-918G= NP_000305.3:n.-918G=
NM_001304717.2:c.-399G= NP_001291646.2:n.-399G=
NM_001304718.1:c.-1623G= NP_001291647.1:n.-1623G=