Canonical Allele Identifier: CA2789011568
Gene: KIF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637633_92637634insACT , CM000672.2:g.92637633_92637634insACT GRCh38
NC_000010.10:g.94397390_94397391insACT , CM000672.1:g.94397390_94397391insACT GRCh37
NC_000010.9:g.94387370_94387371insACT NCBI36
NG_032580.1:g.49566_49567insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2160+88_2160+89insACT MANE Select ENSP00000260731.3:n.2160+88_2160+89insACT
ENST00000676621.1:c.*678+88_*678+89insACT ENSP00000503639.1:n.*678+88_*678+89insACT
ENST00000676647.1:c.1953+88_1953+89insACT ENSP00000503394.1:n.1953+88_1953+89insACT
ENST00000676757.1:c.1953+88_1953+89insACT ENSP00000504289.1:n.1953+88_1953+89insACT
ENST00000677720.1:c.*134+88_*134+89insACT ENSP00000504840.1:n.*134+88_*134+89insACT
ENST00000260731.4:c.2160+88_2160+89insACT ENSP00000260731.3:n.2160+88_2160+89insACT
NM_004523.3:c.2160+88_2160+89insACT NP_004514.2:n.2160+88_2160+89insACT
NM_004523.4:c.2160+88_2160+89insACT MANE Select NP_004514.2:n.2160+88_2160+89insACT