Canonical Allele Identifier: CA595265867
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2789205
ClinVar RCV Id: RCV003666728
dbSNP Id: rs751829354
gnomAD v2: 10-94397317-G-C
gnomAD v4: 10-92637560-G-C
MyVariant Identifiers: chr10:g.94397317G>C (hg19) chr10:g.92637560G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637560G>C , CM000672.2:g.92637560G>C GRCh38
NC_000010.10:g.94397317G>C , CM000672.1:g.94397317G>C GRCh37
NC_000010.9:g.94387297G>C NCBI36
NG_032580.1:g.49493G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2160+15G>C MANE Select ENSP00000260731.3:n.2160+15G>C
ENST00000676621.1:c.*678+15G>C ENSP00000503639.1:n.*678+15G>C
ENST00000676647.1:c.1953+15G>C ENSP00000503394.1:n.1953+15G>C
ENST00000676757.1:c.1953+15G>C ENSP00000504289.1:n.1953+15G>C
ENST00000677720.1:c.*134+15G>C ENSP00000504840.1:n.*134+15G>C
ENST00000260731.4:c.2160+15G>C ENSP00000260731.3:n.2160+15G>C
NM_004523.3:c.2160+15G>C NP_004514.2:n.2160+15G>C
NM_004523.4:c.2160+15G>C MANE Select NP_004514.2:n.2160+15G>C
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