Canonical Allele Identifier: CA211452480
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

ClinVar Variation Id: 488863
ClinVar RCV Id: RCV000579025
dbSNP Id: rs972890157
MyVariant Identifiers: chr10:g.89623234G>C (hg19) chr10:g.87863477G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863477G>C , CM000672.2:g.87863477G>C GRCh38
NC_000010.10:g.89623234G>C , CM000672.1:g.89623234G>C GRCh37
NC_000010.9:g.89613214G>C NCBI36
NG_007466.2:g.5040G>C , LRG_311:g.5040G>C
NG_033079.1:g.4961C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+835G>C (PTEN) ENSP00000516674.1:n.-17+835G>C
ENST00000688308.1:c.-17+364G>C (PTEN) ENSP00000508752.1:n.-17+364G>C
ENST00000693560.1:c.-473G>C (PTEN) ENSP00000509861.1:n.-473G>C
ENST00000445946.5:c.-990C>G (KLLN) MANE Select ENSP00000392204.2:n.-990C>G
ENST00000371953.7:c.-993G>C (PTEN) ENSP00000361021.3:n.-993G>C
ENST00000610634.1:c.-1095G>C (PTEN) ENSP00000477517.1:n.-1095G>C
NM_000314.5:c.-992G>C (PTEN) NP_000305.3:n.-992G>C
NM_000314.6:c.-992G>C (PTEN) NP_000305.3:n.-992G>C
NM_001304717.2:c.-473G>C (PTEN) NP_001291646.2:n.-473G>C
NM_001304718.1:c.-1697G>C (PTEN) NP_001291647.1:n.-1697G>C
NM_001126049.2:c.-990C>G (KLLN) MANE Select NP_001119521.1:n.-990C>G
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