Canonical Allele Identifier: CA2573145840
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388223
ClinVar RCV Id: RCV001877890
dbSNP Id: rs2135923385
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645446_92645447del , CM000672.2:g.92645446_92645447del GRCh38
NC_000010.10:g.94405203_94405204del , CM000672.1:g.94405203_94405204del GRCh37
NC_000010.9:g.94395183_94395184del NCBI36
NG_032580.1:g.57379_57380del

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.2351_2352del MANE Select ENSP00000260731.3:p.Arg784LysfsTer3
ENST00000676621.1:c.*869_*870del ENSP00000503639.1:n.*869_*870del
ENST00000676647.1:c.2144_2145del ENSP00000503394.1:p.Arg715LysfsTer3
ENST00000676757.1:c.2144_2145del ENSP00000504289.1:p.Arg715LysfsTer3
ENST00000677720.1:c.*325_*326del ENSP00000504840.1:n.*325_*326del
ENST00000260731.4:c.2351_2352del ENSP00000260731.3:p.Arg784LysfsTer3
NM_004523.3:c.2351_2352del NP_004514.2:p.Arg784LysfsTer3
NM_004523.4:c.2351_2352del MANE Select NP_004514.2:p.Arg784LysfsTer3
Search 100 bp 5'
Search 100 bp 3'