Canonical Allele Identifier: CA377594307
Gene: KIF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94405322A>C (hg19) chr10:g.92645565A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645565A>C , CM000672.2:g.92645565A>C GRCh38
NC_000010.10:g.94405322A>C , CM000672.1:g.94405322A>C GRCh37
NC_000010.9:g.94395302A>C NCBI36
NG_032580.1:g.57498A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2470A>C MANE Select ENSP00000260731.3:p.Thr824Pro
ENST00000676621.1:c.*988A>C ENSP00000503639.1:n.*988A>C
ENST00000676647.1:c.2263A>C ENSP00000503394.1:p.Thr755Pro
ENST00000676757.1:c.2263A>C ENSP00000504289.1:p.Thr755Pro
ENST00000677720.1:c.*444A>C ENSP00000504840.1:n.*444A>C
ENST00000260731.4:c.2470A>C ENSP00000260731.3:p.Thr824Pro
NM_004523.3:c.2470A>C NP_004514.2:p.Thr824Pro
NM_004523.4:c.2470A>C MANE Select NP_004514.2:p.Thr824Pro
Search 100 bp 5'
Search 100 bp 3'