Canonical Allele Identifier: CA1139768729
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863275_87863286del , CM000672.2:g.87863275_87863286del GRCh38
NC_000010.10:g.89623032_89623043del , CM000672.1:g.89623032_89623043del GRCh37
NC_000010.9:g.89613012_89613023del NCBI36
NG_007466.2:g.4838_4849del , LRG_311:g.4838_4849del
NG_033079.1:g.5152_5163del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+633_-17+644del (PTEN) ENSP00000516674.1:n.-17+633_-17+644del
ENST00000688308.1:c.-17+162_-17+173del (PTEN) ENSP00000508752.1:n.-17+162_-17+173del
ENST00000445946.5:c.-799_-788del (KLLN) MANE Select ENSP00000392204.2:n.-799_-788del
ENST00000371953.7:c.-1195_-1184del (PTEN) ENSP00000361021.3:n.-1195_-1184del
ENST00000445946.3:c.-799_-788del (KLLN) ENSP00000392204.2:n.-799_-788del
NM_001126049.1:c.-799_-788del (KLLN) NP_001119521.1:n.-799_-788del
NM_001126049.2:c.-799_-788del (KLLN) MANE Select NP_001119521.1:n.-799_-788del
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