Canonical Allele Identifier: CA470784925
Gene: KIF11 HGNC NCBI

Linked Data

dbSNP Id: rs1844819575
MyVariant Identifiers: chr10:g.94397266T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637509T>C , CM000672.2:g.92637509T>C GRCh38
NC_000010.10:g.94397266T>C , CM000672.1:g.94397266T>C GRCh37
NC_000010.9:g.94387246T>C NCBI36
NG_032580.1:g.49442T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2124T>C MANE Select ENSP00000260731.3:p.Thr708=
ENST00000676621.1:c.*642T>C ENSP00000503639.1:n.*642T>C
ENST00000676647.1:c.1917T>C ENSP00000503394.1:p.Thr639=
ENST00000676757.1:c.1917T>C ENSP00000504289.1:p.Thr639=
ENST00000677720.1:c.*98T>C ENSP00000504840.1:n.*98T>C
ENST00000260731.4:c.2124T>C ENSP00000260731.3:p.Thr708=
NM_004523.3:c.2124T>C NP_004514.2:p.Thr708=
NM_004523.4:c.2124T>C MANE Select NP_004514.2:p.Thr708=
Search 100 bp 5'
Search 100 bp 3'