Canonical Allele Identifier: CA470982728
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347011
ClinVar RCV Id: RCV002050253
dbSNP Id: rs2135923378
MyVariant Identifiers: chr10:g.94405195G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92645438G>A , CM000672.2:g.92645438G>A GRCh38
NC_000010.10:g.94405195G>A , CM000672.1:g.94405195G>A GRCh37
NC_000010.9:g.94395175G>A NCBI36
NG_032580.1:g.57371G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.2343G>A MANE Select ENSP00000260731.3:p.Gln781=
ENST00000676621.1:c.*861G>A ENSP00000503639.1:n.*861G>A
ENST00000676647.1:c.2136G>A ENSP00000503394.1:p.Gln712=
ENST00000676757.1:c.2136G>A ENSP00000504289.1:p.Gln712=
ENST00000677720.1:c.*317G>A ENSP00000504840.1:n.*317G>A
ENST00000260731.4:c.2343G>A ENSP00000260731.3:p.Gln781=
NM_004523.3:c.2343G>A NP_004514.2:p.Gln781=
NM_004523.4:c.2343G>A MANE Select NP_004514.2:p.Gln781=
Search 100 bp 5'
Search 100 bp 3'