Canonical Allele Identifier: CA1926143086
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863545G= , CM000672.2:g.87863545G= GRCh38
NC_000010.10:g.89623302G= , CM000672.1:g.89623302G= GRCh37
NC_000010.9:g.89613282G= NCBI36
NG_007466.2:g.5108G= , LRG_311:g.5108G=
NG_033079.1:g.4893C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+903G= ENSP00000516674.1:n.-17+903G=
ENST00000688308.1:c.-17+432G= ENSP00000508752.1:n.-17+432G=
ENST00000693560.1:c.-405G= ENSP00000509861.1:n.-405G=
ENST00000371953.7:c.-925G= ENSP00000361021.3:n.-925G=
ENST00000610634.1:c.-1027G= ENSP00000477517.1:n.-1027G=
NM_000314.5:c.-924G= NP_000305.3:n.-924G=
NM_000314.6:c.-924G= NP_000305.3:n.-924G=
NM_001304717.2:c.-405G= NP_001291646.2:n.-405G=
NM_001304718.1:c.-1629G= NP_001291647.1:n.-1629G=