Canonical Allele Identifier: CA16605735
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 392999
dbSNP Id: rs1057524736

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92593453G>A , CM000672.2:g.92593453G>A GRCh38
NC_000010.10:g.94353210G>A , CM000672.1:g.94353210G>A GRCh37
NC_000010.9:g.94343190G>A NCBI36
NG_032580.1:g.5386G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.77+1G>A MANE Select ENSP00000260731.3:n.77+1G>A
ENST00000676621.1:c.77+1G>A ENSP00000503639.1:n.77+1G>A
ENST00000676647.1:c.-131+1624G>A ENSP00000503394.1:n.-131+1624G>A
ENST00000676757.1:c.-130-12812G>A ENSP00000504289.1:n.-130-12812G>A
ENST00000677720.1:c.77+1G>A ENSP00000504840.1:n.77+1G>A
ENST00000260731.4:c.77+1G>A ENSP00000260731.3:n.77+1G>A
NM_004523.3:c.77+1G>A NP_004514.2:n.77+1G>A
NM_004523.4:c.77+1G>A MANE Select NP_004514.2:n.77+1G>A