Canonical Allele Identifier: CA2571229707
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 1760543
ClinVar RCV Id: RCV002409762
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863693G>A , CM000672.2:g.87863693G>A GRCh38
NC_000010.10:g.89623450G>A , CM000672.1:g.89623450G>A GRCh37
NC_000010.9:g.89613430G>A NCBI36
NG_007466.2:g.5256G>A , LRG_311:g.5256G>A
NG_033079.1:g.4745C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-777G>A ENSP00000514759.2:n.-777G>A
ENST00000710265.1:c.-777G>A ENSP00000518161.1:n.-777G>A
ENST00000706954.1:c.-16-761G>A ENSP00000516674.1:n.-16-761G>A
ENST00000706955.1:c.-777G>A ENSP00000516675.1:n.-777G>A
ENST00000688158.1:c.-777G>A ENSP00000509254.1:n.-777G>A
ENST00000688308.1:c.-17+580G>A ENSP00000508752.1:n.-17+580G>A
ENST00000693560.1:c.-257G>A ENSP00000509861.1:n.-257G>A
ENST00000371953.8:c.-777G>A MANE Select ENSP00000361021.3:n.-777G>A
ENST00000371953.7:c.-777G>A ENSP00000361021.3:n.-777G>A
ENST00000610634.1:c.-879G>A ENSP00000477517.1:n.-879G>A
NM_000314.5:c.-776G>A NP_000305.3:n.-776G>A
NM_000314.6:c.-776G>A NP_000305.3:n.-776G>A
NM_001304717.2:c.-257G>A NP_001291646.2:n.-257G>A
NM_001304718.1:c.-1481G>A NP_001291647.1:n.-1481G>A
NM_000314.7:c.-776G>A NP_000305.3:n.-776G>A
NM_001304717.5:c.-257G>A NP_001291646.4:n.-257G>A
NM_001304718.2:c.-1481G>A NP_001291647.1:n.-1481G>A
NM_000314.8:c.-777G>A MANE Select NP_000305.3:n.-777G>A
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