Canonical Allele Identifier: CA377594009
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2270619
ClinVar RCV Id: RCV002809602
gnomAD v4: 10-92645436-C-G
COSMIC: COSM5581474
MyVariant Identifiers: chr10:g.94405193C>G (hg19) chr10:g.92645436C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645436C>G , CM000672.2:g.92645436C>G GRCh38
NC_000010.10:g.94405193C>G , CM000672.1:g.94405193C>G GRCh37
NC_000010.9:g.94395173C>G NCBI36
NG_032580.1:g.57369C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.2341C>G MANE Select ENSP00000260731.3:p.Gln781Glu
ENST00000676621.1:c.*859C>G ENSP00000503639.1:n.*859C>G
ENST00000676647.1:c.2134C>G ENSP00000503394.1:p.Gln712Glu
ENST00000676757.1:c.2134C>G ENSP00000504289.1:p.Gln712Glu
ENST00000677720.1:c.*315C>G ENSP00000504840.1:n.*315C>G
ENST00000260731.4:c.2341C>G ENSP00000260731.3:p.Gln781Glu
NM_004523.3:c.2341C>G NP_004514.2:p.Gln781Glu
NM_004523.4:c.2341C>G MANE Select NP_004514.2:p.Gln781Glu
Search 100 bp 5'
Search 100 bp 3'