Canonical Allele Identifier: CA211451859
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

dbSNP Id: rs781249764
gnomAD v3: 10-87863111-C-T
gnomAD v4: 10-87863111-C-T
MyVariant Identifiers: chr10:g.89622868C>T (hg19) chr10:g.87863111C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863111C>T , CM000672.2:g.87863111C>T GRCh38
NC_000010.10:g.89622868C>T , CM000672.1:g.89622868C>T GRCh37
NC_000010.9:g.89612848C>T NCBI36
NG_007466.2:g.4674C>T , LRG_311:g.4674C>T
NG_033079.1:g.5327G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+469C>T (PTEN) ENSP00000516674.1:n.-17+469C>T
ENST00000688308.1:c.-19C>T (PTEN) ENSP00000508752.1:n.-19C>T
ENST00000445946.5:c.-624G>A (KLLN) MANE Select ENSP00000392204.2:n.-624G>A
ENST00000445946.3:c.-624G>A (KLLN) ENSP00000392204.2:n.-624G>A
NM_001126049.1:c.-624G>A (KLLN) NP_001119521.1:n.-624G>A
NM_001126049.2:c.-624G>A (KLLN) MANE Select NP_001119521.1:n.-624G>A
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