Canonical Allele Identifier: CA377594132
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513211
ClinVar RCV Id: RCV002045854
dbSNP Id: rs2135923418
gnomAD v4: 10-92645490-A-G
MyVariant Identifiers: chr10:g.94405247A>G (hg19) chr10:g.92645490A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645490A>G , CM000672.2:g.92645490A>G GRCh38
NC_000010.10:g.94405247A>G , CM000672.1:g.94405247A>G GRCh37
NC_000010.9:g.94395227A>G NCBI36
NG_032580.1:g.57423A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2395A>G MANE Select ENSP00000260731.3:p.Lys799Glu
ENST00000676621.1:c.*913A>G ENSP00000503639.1:n.*913A>G
ENST00000676647.1:c.2188A>G ENSP00000503394.1:p.Lys730Glu
ENST00000676757.1:c.2188A>G ENSP00000504289.1:p.Lys730Glu
ENST00000677720.1:c.*369A>G ENSP00000504840.1:n.*369A>G
ENST00000260731.4:c.2395A>G ENSP00000260731.3:p.Lys799Glu
NM_004523.3:c.2395A>G NP_004514.2:p.Lys799Glu
NM_004523.4:c.2395A>G MANE Select NP_004514.2:p.Lys799Glu
Search 100 bp 5'
Search 100 bp 3'