Canonical Allele Identifier: CA2610046164
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

gnomAD v4: 10-87863440-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863444del , CM000672.2:g.87863444del GRCh38
NC_000010.10:g.89623201del , CM000672.1:g.89623201del GRCh37
NC_000010.9:g.89613181del NCBI36
NG_007466.2:g.5007del , LRG_311:g.5007del
NG_033079.1:g.4997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+802del (PTEN) ENSP00000516674.1:n.-17+802del
ENST00000688308.1:c.-17+331del (PTEN) ENSP00000508752.1:n.-17+331del
ENST00000693560.1:c.-506del (PTEN) ENSP00000509861.1:n.-506del
ENST00000445946.5:c.-954del (KLLN) MANE Select ENSP00000392204.2:n.-954del
ENST00000371953.7:c.-1026del (PTEN) ENSP00000361021.3:n.-1026del
ENST00000610634.1:c.-1128del (PTEN) ENSP00000477517.1:n.-1128del
NM_000314.5:c.-1025del (PTEN) NP_000305.3:n.-1025del
NM_000314.6:c.-1025del (PTEN) NP_000305.3:n.-1025del
NM_001304717.2:c.-506del (PTEN) NP_001291646.2:n.-506del
NM_001304718.1:c.-1730del (PTEN) NP_001291647.1:n.-1730del
NM_001126049.2:c.-954del (KLLN) MANE Select NP_001119521.1:n.-954del
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