Canonical Allele Identifier: CA470784927
Gene: KIF11 HGNC NCBI

Linked Data

dbSNP Id: rs2135919295
MyVariant Identifiers: chr10:g.94397273C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637516C>T , CM000672.2:g.92637516C>T GRCh38
NC_000010.10:g.94397273C>T , CM000672.1:g.94397273C>T GRCh37
NC_000010.9:g.94387253C>T NCBI36
NG_032580.1:g.49449C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2131C>T MANE Select ENSP00000260731.3:p.Leu711=
ENST00000676621.1:c.*649C>T ENSP00000503639.1:n.*649C>T
ENST00000676647.1:c.1924C>T ENSP00000503394.1:p.Leu642=
ENST00000676757.1:c.1924C>T ENSP00000504289.1:p.Leu642=
ENST00000677720.1:c.*105C>T ENSP00000504840.1:n.*105C>T
ENST00000260731.4:c.2131C>T ENSP00000260731.3:p.Leu711=
NM_004523.3:c.2131C>T NP_004514.2:p.Leu711=
NM_004523.4:c.2131C>T MANE Select NP_004514.2:p.Leu711=