Canonical Allele Identifier: CA16043624
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 374219
ClinVar RCV Id: RCV000415366
dbSNP Id: rs1057518980
MyVariant Identifiers: chr10:g.94373206_94373215del (hg19) chr10:g.92613449_92613458del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92613449_92613458del , CM000672.2:g.92613449_92613458del GRCh38
NC_000010.10:g.94373206_94373215del , CM000672.1:g.94373206_94373215del GRCh37
NC_000010.9:g.94363186_94363195del NCBI36
NG_032580.1:g.25382_25391del

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.862_871del MANE Select ENSP00000260731.3:p.Ile288ProfsTer3
ENST00000676621.1:c.862_871del ENSP00000503639.1:p.Ile288ProfsTer3
ENST00000676647.1:c.655_664del ENSP00000503394.1:p.Ile219ProfsTer3
ENST00000676757.1:c.655_664del ENSP00000504289.1:p.Ile219ProfsTer3
ENST00000677720.1:c.862_871del ENSP00000504840.1:p.Ile288ProfsTer3
ENST00000260731.4:c.862_871del ENSP00000260731.3:p.Ile288ProfsTer3
NM_004523.3:c.862_871del NP_004514.2:p.Ile288ProfsTer3
NM_004523.4:c.862_871del MANE Select NP_004514.2:p.Ile288ProfsTer3
Search 100 bp 5'
Search 100 bp 3'