Canonical Allele Identifier: CA470784902
Gene: KIF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94397231T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637474T>C , CM000672.2:g.92637474T>C GRCh38
NC_000010.10:g.94397231T>C , CM000672.1:g.94397231T>C GRCh37
NC_000010.9:g.94387211T>C NCBI36
NG_032580.1:g.49407T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2089T>C MANE Select ENSP00000260731.3:p.Leu697=
ENST00000676621.1:c.*607T>C ENSP00000503639.1:n.*607T>C
ENST00000676647.1:c.1882T>C ENSP00000503394.1:p.Leu628=
ENST00000676757.1:c.1882T>C ENSP00000504289.1:p.Leu628=
ENST00000677720.1:c.*63T>C ENSP00000504840.1:n.*63T>C
ENST00000260731.4:c.2089T>C ENSP00000260731.3:p.Leu697=
NM_004523.3:c.2089T>C NP_004514.2:p.Leu697=
NM_004523.4:c.2089T>C MANE Select NP_004514.2:p.Leu697=
Search 100 bp 5'
Search 100 bp 3'