Canonical Allele Identifier: CA470784921
Gene: KIF11 HGNC NCBI

Linked Data

dbSNP Id: rs1844819485
MyVariant Identifiers: chr10:g.94397263A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637506A>G , CM000672.2:g.92637506A>G GRCh38
NC_000010.10:g.94397263A>G , CM000672.1:g.94397263A>G GRCh37
NC_000010.9:g.94387243A>G NCBI36
NG_032580.1:g.49439A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2121A>G MANE Select ENSP00000260731.3:p.Leu707=
ENST00000676621.1:c.*639A>G ENSP00000503639.1:n.*639A>G
ENST00000676647.1:c.1914A>G ENSP00000503394.1:p.Leu638=
ENST00000676757.1:c.1914A>G ENSP00000504289.1:p.Leu638=
ENST00000677720.1:c.*95A>G ENSP00000504840.1:n.*95A>G
ENST00000260731.4:c.2121A>G ENSP00000260731.3:p.Leu707=
NM_004523.3:c.2121A>G NP_004514.2:p.Leu707=
NM_004523.4:c.2121A>G MANE Select NP_004514.2:p.Leu707=