Canonical Allele Identifier: CA5603922

Gene: KIF11

Linked Data

• ClinVar Variation Id: 963518
• ClinVar RCV Id: RCV001237555 ; RCV001331252 ; RCV001819934 ; RCV002563892
• dbSNP Id: rs200410468
• ExAC: 10:94366137 A / G
• gnomAD v2: 10-94366137-A-G
• gnomAD v3: 10-92606380-A-G
• gnomAD v4: 10-92606380-A-G
• MyVariant Identifiers: chr10:g.94366137A>G (hg19) ; chr10:g.92606380A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92606380A>G , CM000672.2:g.92606380A>G	GRCh38
NC_000010.10:g.94366137A>G , CM000672.1:g.94366137A>G	GRCh37
NC_000010.9:g.94356117A>G	NCBI36
NG_032580.1:g.18313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260731.5:c.193A>G MANE Select	ENSP00000260731.3:p.Thr65Ala
ENST00000676621.1:c.193A>G	ENSP00000503639.1:p.Thr65Ala
ENST00000676647.1:c.-15A>G	ENSP00000503394.1:n.-15A>G
ENST00000676757.1:c.-15A>G	ENSP00000504289.1:n.-15A>G
ENST00000677720.1:c.193A>G	ENSP00000504840.1:p.Thr65Ala
ENST00000260731.4:c.193A>G	ENSP00000260731.3:p.Thr65Ala
NM_004523.3:c.193A>G	NP_004514.2:p.Thr65Ala
NM_004523.4:c.193A>G MANE Select	NP_004514.2:p.Thr65Ala