Canonical Allele Identifier: CA1928269248
Gene: KIF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645436C= , CM000672.2:g.92645436C= GRCh38
NC_000010.10:g.94405193C= , CM000672.1:g.94405193C= GRCh37
NC_000010.9:g.94395173C= NCBI36
NG_032580.1:g.57369C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.2341C= MANE Select ENSP00000260731.3:p.Gln781=
ENST00000676621.1:c.*859C= ENSP00000503639.1:n.*859C=
ENST00000676647.1:c.2134C= ENSP00000503394.1:p.Gln712=
ENST00000676757.1:c.2134C= ENSP00000504289.1:p.Gln712=
ENST00000677720.1:c.*315C= ENSP00000504840.1:n.*315C=
ENST00000260731.4:c.2341C= ENSP00000260731.3:p.Gln781=
NM_004523.3:c.2341C= NP_004514.2:p.Gln781=
NM_004523.4:c.2341C= MANE Select NP_004514.2:p.Gln781=