Canonical Allele Identifier: CA470781094
Gene: KIF11 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92593420G>A , CM000672.2:g.92593420G>A GRCh38
NC_000010.10:g.94353177G>A , CM000672.1:g.94353177G>A GRCh37
NC_000010.9:g.94343157G>A NCBI36
NG_032580.1:g.5353G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.45G>A MANE Select ENSP00000260731.3:p.Lys15=
ENST00000676621.1:c.45G>A ENSP00000503639.1:p.Lys15=
ENST00000676647.1:c.-131+1591G>A ENSP00000503394.1:n.-131+1591G>A
ENST00000676757.1:c.-130-12845G>A ENSP00000504289.1:n.-130-12845G>A
ENST00000677720.1:c.45G>A ENSP00000504840.1:p.Lys15=
ENST00000260731.4:c.45G>A ENSP00000260731.3:p.Lys15=
NM_004523.3:c.45G>A NP_004514.2:p.Lys15=
NM_004523.4:c.45G>A MANE Select NP_004514.2:p.Lys15=