Canonical Allele Identifier: CA2610045276
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

gnomAD v4: 10-87863021-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863021A>T , CM000672.2:g.87863021A>T GRCh38
NC_000010.10:g.89622778A>T , CM000672.1:g.89622778A>T GRCh37
NC_000010.9:g.89612758A>T NCBI36
NG_007466.2:g.4584A>T , LRG_311:g.4584A>T
NG_033079.1:g.5417T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+379A>T (PTEN) ENSP00000516674.1:n.-17+379A>T
ENST00000688308.1:c.-109A>T (PTEN) ENSP00000508752.1:n.-109A>T
ENST00000445946.5:c.-534T>A (KLLN) MANE Select ENSP00000392204.2:n.-534T>A
ENST00000445946.3:c.-534T>A (KLLN) ENSP00000392204.2:n.-534T>A
NM_001126049.1:c.-534T>A (KLLN) NP_001119521.1:n.-534T>A
NM_001126049.2:c.-534T>A (KLLN) MANE Select NP_001119521.1:n.-534T>A
Search 100 bp 5'
Search 100 bp 3'