Canonical Allele Identifier: CA211514015
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1961840
ClinVar RCV Id: RCV002720983 RCV003455563
dbSNP Id: rs989824359
gnomAD v2: 10-94397307-G-A
gnomAD v4: 10-92637550-G-A
MyVariant Identifiers: chr10:g.94397307G>A (hg19) chr10:g.92637550G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637550G>A , CM000672.2:g.92637550G>A GRCh38
NC_000010.10:g.94397307G>A , CM000672.1:g.94397307G>A GRCh37
NC_000010.9:g.94387287G>A NCBI36
NG_032580.1:g.49483G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2160+5G>A MANE Select ENSP00000260731.3:n.2160+5G>A
ENST00000676621.1:c.*678+5G>A ENSP00000503639.1:n.*678+5G>A
ENST00000676647.1:c.1953+5G>A ENSP00000503394.1:n.1953+5G>A
ENST00000676757.1:c.1953+5G>A ENSP00000504289.1:n.1953+5G>A
ENST00000677720.1:c.*134+5G>A ENSP00000504840.1:n.*134+5G>A
ENST00000260731.4:c.2160+5G>A ENSP00000260731.3:n.2160+5G>A
NM_004523.3:c.2160+5G>A NP_004514.2:n.2160+5G>A
NM_004523.4:c.2160+5G>A MANE Select NP_004514.2:n.2160+5G>A
Search 100 bp 5'
Search 100 bp 3'