Canonical Allele Identifier: CA377594128
Gene: KIF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94405245T>A (hg19) chr10:g.92645488T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645488T>A , CM000672.2:g.92645488T>A GRCh38
NC_000010.10:g.94405245T>A , CM000672.1:g.94405245T>A GRCh37
NC_000010.9:g.94395225T>A NCBI36
NG_032580.1:g.57421T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2393T>A MANE Select ENSP00000260731.3:p.Val798Glu
ENST00000676621.1:c.*911T>A ENSP00000503639.1:n.*911T>A
ENST00000676647.1:c.2186T>A ENSP00000503394.1:p.Val729Glu
ENST00000676757.1:c.2186T>A ENSP00000504289.1:p.Val729Glu
ENST00000677720.1:c.*367T>A ENSP00000504840.1:n.*367T>A
ENST00000260731.4:c.2393T>A ENSP00000260731.3:p.Val798Glu
NM_004523.3:c.2393T>A NP_004514.2:p.Val798Glu
NM_004523.4:c.2393T>A MANE Select NP_004514.2:p.Val798Glu
Search 100 bp 5'
Search 100 bp 3'