Canonical Allele Identifier: CA470982729
Gene: KIF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94405198A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645441A>G , CM000672.2:g.92645441A>G GRCh38
NC_000010.10:g.94405198A>G , CM000672.1:g.94405198A>G GRCh37
NC_000010.9:g.94395178A>G NCBI36
NG_032580.1:g.57374A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.2346A>G MANE Select ENSP00000260731.3:p.Glu782=
ENST00000676621.1:c.*864A>G ENSP00000503639.1:n.*864A>G
ENST00000676647.1:c.2139A>G ENSP00000503394.1:p.Glu713=
ENST00000676757.1:c.2139A>G ENSP00000504289.1:p.Glu713=
ENST00000677720.1:c.*320A>G ENSP00000504840.1:n.*320A>G
ENST00000260731.4:c.2346A>G ENSP00000260731.3:p.Glu782=
NM_004523.3:c.2346A>G NP_004514.2:p.Glu782=
NM_004523.4:c.2346A>G MANE Select NP_004514.2:p.Glu782=