Canonical Allele Identifier: CA658683607
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

ClinVar Variation Id: 488930
ClinVar RCV Id: RCV000578872
dbSNP Id: rs1554889854
gnomAD v4: 10-87863360-G-T
MyVariant Identifiers: chr10:g.89623117G>T (hg19) chr10:g.87863360G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863360G>T , CM000672.2:g.87863360G>T GRCh38
NC_000010.10:g.89623117G>T , CM000672.1:g.89623117G>T GRCh37
NC_000010.9:g.89613097G>T NCBI36
NG_007466.2:g.4923G>T , LRG_311:g.4923G>T
NG_033079.1:g.5078C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+718G>T (PTEN) ENSP00000516674.1:n.-17+718G>T
ENST00000688308.1:c.-17+247G>T (PTEN) ENSP00000508752.1:n.-17+247G>T
ENST00000445946.5:c.-873C>A (KLLN) MANE Select ENSP00000392204.2:n.-873C>A
ENST00000371953.7:c.-1110G>T (PTEN) ENSP00000361021.3:n.-1110G>T
ENST00000445946.3:c.-873C>A (KLLN) ENSP00000392204.2:n.-873C>A
NM_001126049.1:c.-873C>A (KLLN) NP_001119521.1:n.-873C>A
NM_001126049.2:c.-873C>A (KLLN) MANE Select NP_001119521.1:n.-873C>A
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