Canonical Allele Identifier: CA205761
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 211271
ClinVar RCV Id: RCV000192737
dbSNP Id: rs797045649
MyVariant Identifiers: chr10:g.94353132_94353134delinsAA (hg19) chr10:g.92593375_92593377delinsAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92593375_92593377delinsAA , CM000672.2:g.92593375_92593377delinsAA GRCh38
NC_000010.10:g.94353132_94353134delinsAA , CM000672.1:g.94353132_94353134delinsAA GRCh37
NC_000010.9:g.94343112_94343114delinsAA NCBI36
NG_032580.1:g.5308_5310delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.-1_2delinsAA
ENST00000676621.1:c.-1_2delinsAA
ENST00000676647.1:c.-131+1546_-131+1548delinsAA ENSP00000503394.1:n.-131+1546_-131+1548delinsAA
ENST00000676757.1:c.-130-12890_-130-12888delinsAA ENSP00000504289.1:n.-130-12890_-130-12888delinsAA
ENST00000677720.1:c.-1_2delinsAA
ENST00000260731.4:c.-1_2delinsAA
NM_004523.3:c.-1_2delinsAA
NM_004523.4:c.-1_2delinsAA
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