Canonical Allele Identifier: CA2610046459
Gene: PTEN HGNC NCBI

Linked Data

gnomAD v4: 10-87863695-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863695C>A , CM000672.2:g.87863695C>A GRCh38
NC_000010.10:g.89623452C>A , CM000672.1:g.89623452C>A GRCh37
NC_000010.9:g.89613432C>A NCBI36
NG_007466.2:g.5258C>A , LRG_311:g.5258C>A
NG_033079.1:g.4743G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-775C>A ENSP00000514759.2:n.-775C>A
ENST00000710265.1:c.-775C>A ENSP00000518161.1:n.-775C>A
ENST00000706954.1:c.-16-759C>A ENSP00000516674.1:n.-16-759C>A
ENST00000706955.1:c.-775C>A ENSP00000516675.1:n.-775C>A
ENST00000688158.1:c.-775C>A ENSP00000509254.1:n.-775C>A
ENST00000688308.1:c.-17+582C>A ENSP00000508752.1:n.-17+582C>A
ENST00000693560.1:c.-255C>A ENSP00000509861.1:n.-255C>A
ENST00000371953.8:c.-775C>A MANE Select ENSP00000361021.3:n.-775C>A
ENST00000371953.7:c.-775C>A ENSP00000361021.3:n.-775C>A
ENST00000610634.1:c.-877C>A ENSP00000477517.1:n.-877C>A
NM_000314.5:c.-774C>A NP_000305.3:n.-774C>A
NM_000314.6:c.-774C>A NP_000305.3:n.-774C>A
NM_001304717.2:c.-255C>A NP_001291646.2:n.-255C>A
NM_001304718.1:c.-1479C>A NP_001291647.1:n.-1479C>A
NM_000314.7:c.-774C>A NP_000305.3:n.-774C>A
NM_001304717.5:c.-255C>A NP_001291646.4:n.-255C>A
NM_001304718.2:c.-1479C>A NP_001291647.1:n.-1479C>A
NM_000314.8:c.-775C>A MANE Select NP_000305.3:n.-775C>A
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