Canonical Allele Identifier: CA377593366

Gene: KIF11

Linked Data

• ClinVar Variation Id: 1521825
• ClinVar RCV Id: RCV002027981
• dbSNP Id: rs1844818700
• MyVariant Identifiers: chr10:g.94397220C>G (hg19) ; chr10:g.92637463C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92637463C>G , CM000672.2:g.92637463C>G	GRCh38
NC_000010.10:g.94397220C>G , CM000672.1:g.94397220C>G	GRCh37
NC_000010.9:g.94387200C>G	NCBI36
NG_032580.1:g.49396C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260731.5:c.2078C>G MANE Select	ENSP00000260731.3:p.Thr693Ser
ENST00000676621.1:c.*596C>G	ENSP00000503639.1:n.*596C>G
ENST00000676647.1:c.1871C>G	ENSP00000503394.1:p.Thr624Ser
ENST00000676757.1:c.1871C>G	ENSP00000504289.1:p.Thr624Ser
ENST00000677720.1:c.*52C>G	ENSP00000504840.1:n.*52C>G
ENST00000260731.4:c.2078C>G	ENSP00000260731.3:p.Thr693Ser
NM_004523.3:c.2078C>G	NP_004514.2:p.Thr693Ser
NM_004523.4:c.2078C>G MANE Select	NP_004514.2:p.Thr693Ser