Canonical Allele Identifier: CA1926143099
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863557T= , CM000672.2:g.87863557T= GRCh38
NC_000010.10:g.89623314T= , CM000672.1:g.89623314T= GRCh37
NC_000010.9:g.89613294T= NCBI36
NG_007466.2:g.5120T= , LRG_311:g.5120T=
NG_033079.1:g.4881A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-897T= ENSP00000516674.1:n.-16-897T=
ENST00000688308.1:c.-17+444T= ENSP00000508752.1:n.-17+444T=
ENST00000693560.1:c.-393T= ENSP00000509861.1:n.-393T=
ENST00000371953.7:c.-913T= ENSP00000361021.3:n.-913T=
ENST00000610634.1:c.-1015T= ENSP00000477517.1:n.-1015T=
NM_000314.5:c.-912T= NP_000305.3:n.-912T=
NM_000314.6:c.-912T= NP_000305.3:n.-912T=
NM_001304717.2:c.-393T= NP_001291646.2:n.-393T=
NM_001304718.1:c.-1617T= NP_001291647.1:n.-1617T=