Canonical Allele Identifier: CA470784121

Gene: KIF11

Linked Data

• ClinVar Variation Id: 450271
• ClinVar RCV Id: RCV000523961 ; RCV000787274 ; RCV003987579
• dbSNP Id: rs1554861545
• MyVariant Identifiers: chr10:g.94388641_94388643del (hg19) ; chr10:g.94388635_94388637del (hg19) ; chr10:g.92628884_92628886del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92628884_92628886del , CM000672.2:g.92628884_92628886del	GRCh38
NC_000010.10:g.94388641_94388643del , CM000672.1:g.94388641_94388643del	GRCh37
NC_000010.9:g.94378621_94378623del	NCBI36
NG_032580.1:g.40817_40819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260731.5:c.1294_1296del MANE Select	ENSP00000260731.3:p.Glu432del
ENST00000676621.1:c.1294_1296del	ENSP00000503639.1:p.Glu432del
ENST00000676647.1:c.1087_1089del	ENSP00000503394.1:p.Glu363del
ENST00000676757.1:c.1087_1089del	ENSP00000504289.1:p.Glu363del
ENST00000677720.1:c.1294_1296del	ENSP00000504840.1:p.Glu432del
ENST00000260731.4:c.1294_1296del	ENSP00000260731.3:p.Glu432del
NM_004523.3:c.1294_1296del	NP_004514.2:p.Glu432del
NM_004523.4:c.1294_1296del MANE Select	NP_004514.2:p.Glu432del