Canonical Allele Identifier: CA1928263520
Gene: KIF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637464C= , CM000672.2:g.92637464C= GRCh38
NC_000010.10:g.94397221C= , CM000672.1:g.94397221C= GRCh37
NC_000010.9:g.94387201C= NCBI36
NG_032580.1:g.49397C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2079C= MANE Select ENSP00000260731.3:p.Thr693=
ENST00000676621.1:c.*597C= ENSP00000503639.1:n.*597C=
ENST00000676647.1:c.1872C= ENSP00000503394.1:p.Thr624=
ENST00000676757.1:c.1872C= ENSP00000504289.1:p.Thr624=
ENST00000677720.1:c.*53C= ENSP00000504840.1:n.*53C=
ENST00000260731.4:c.2079C= ENSP00000260731.3:p.Thr693=
NM_004523.3:c.2079C= NP_004514.2:p.Thr693=
NM_004523.4:c.2079C= MANE Select NP_004514.2:p.Thr693=