Canonical Allele Identifier: CA377594020
Gene: KIF11 HGNC NCBI

Linked Data

gnomAD v4: 10-92645441-A-C
MyVariant Identifiers: chr10:g.94405198A>C (hg19) chr10:g.92645441A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.2346A>C MANE Select ENSP00000260731.3:p.Glu782Asp
ENST00000676621.1:c.*864A>C ENSP00000503639.1:n.*864A>C
ENST00000676647.1:c.2139A>C ENSP00000503394.1:p.Glu713Asp
ENST00000676757.1:c.2139A>C ENSP00000504289.1:p.Glu713Asp
ENST00000677720.1:c.*320A>C ENSP00000504840.1:n.*320A>C
ENST00000260731.4:c.2346A>C ENSP00000260731.3:p.Glu782Asp
NM_004523.3:c.2346A>C NP_004514.2:p.Glu782Asp
NM_004523.4:c.2346A>C MANE Select NP_004514.2:p.Glu782Asp
Search 100 bp 5'
Search 100 bp 3'