Canonical Allele Identifier: CA2788894872
Gene: PTEN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863538C>A , CM000672.2:g.87863538C>A GRCh38
NC_000010.10:g.89623295C>A , CM000672.1:g.89623295C>A GRCh37
NC_000010.9:g.89613275C>A NCBI36
NG_007466.2:g.5101C>A , LRG_311:g.5101C>A
NG_033079.1:g.4900G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+896C>A ENSP00000516674.1:n.-17+896C>A
ENST00000688308.1:c.-17+425C>A ENSP00000508752.1:n.-17+425C>A
ENST00000693560.1:c.-412C>A ENSP00000509861.1:n.-412C>A
ENST00000371953.7:c.-932C>A ENSP00000361021.3:n.-932C>A
ENST00000610634.1:c.-1034C>A ENSP00000477517.1:n.-1034C>A
NM_000314.5:c.-931C>A NP_000305.3:n.-931C>A
NM_000314.6:c.-931C>A NP_000305.3:n.-931C>A
NM_001304717.2:c.-412C>A NP_001291646.2:n.-412C>A
NM_001304718.1:c.-1636C>A NP_001291647.1:n.-1636C>A
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