Canonical Allele Identifier: CA377593534
Gene: KIF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94397297T>C (hg19) chr10:g.92637540T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637540T>C , CM000672.2:g.92637540T>C GRCh38
NC_000010.10:g.94397297T>C , CM000672.1:g.94397297T>C GRCh37
NC_000010.9:g.94387277T>C NCBI36
NG_032580.1:g.49473T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2155T>C MANE Select ENSP00000260731.3:p.Ser719Pro
ENST00000676621.1:c.*673T>C ENSP00000503639.1:n.*673T>C
ENST00000676647.1:c.1948T>C ENSP00000503394.1:p.Ser650Pro
ENST00000676757.1:c.1948T>C ENSP00000504289.1:p.Ser650Pro
ENST00000677720.1:c.*129T>C ENSP00000504840.1:n.*129T>C
ENST00000260731.4:c.2155T>C ENSP00000260731.3:p.Ser719Pro
NM_004523.3:c.2155T>C NP_004514.2:p.Ser719Pro
NM_004523.4:c.2155T>C MANE Select NP_004514.2:p.Ser719Pro
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