Canonical Allele Identifier: CA5604546
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1978818
ClinVar RCV Id: RCV002765939
dbSNP Id: rs774066944
ExAC: 10:94413430 A / G
gnomAD v2: 10-94413430-A-G
gnomAD v3: 10-92653673-A-G
gnomAD v4: 10-92653673-A-G
MyVariant Identifiers: chr10:g.94413430A>G (hg19) chr10:g.92653673A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92653673A>G , CM000672.2:g.92653673A>G GRCh38
NC_000010.10:g.94413430A>G , CM000672.1:g.94413430A>G GRCh37
NC_000010.9:g.94403410A>G NCBI36
NG_032580.1:g.65606A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.3048A>G MANE Select ENSP00000260731.3:p.Lys1016=
ENST00000676621.1:c.*1566A>G ENSP00000503639.1:n.*1566A>G
ENST00000676647.1:c.2841A>G ENSP00000503394.1:p.Lys947=
ENST00000676757.1:c.2841A>G ENSP00000504289.1:p.Lys947=
ENST00000677720.1:c.*1022A>G ENSP00000504840.1:n.*1022A>G
ENST00000260731.4:c.3048A>G ENSP00000260731.3:p.Lys1016=
NM_004523.3:c.3048A>G NP_004514.2:p.Lys1016=
NM_004523.4:c.3048A>G MANE Select NP_004514.2:p.Lys1016=
Search 100 bp 5'
Search 100 bp 3'