Canonical Allele Identifier: CA470784914
Gene: KIF11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.94397248G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92637491G>A , CM000672.2:g.92637491G>A GRCh38
NC_000010.10:g.94397248G>A , CM000672.1:g.94397248G>A GRCh37
NC_000010.9:g.94387228G>A NCBI36
NG_032580.1:g.49424G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260731.5:c.2106G>A MANE Select ENSP00000260731.3:p.Lys702=
ENST00000676621.1:c.*624G>A ENSP00000503639.1:n.*624G>A
ENST00000676647.1:c.1899G>A ENSP00000503394.1:p.Lys633=
ENST00000676757.1:c.1899G>A ENSP00000504289.1:p.Lys633=
ENST00000677720.1:c.*80G>A ENSP00000504840.1:n.*80G>A
ENST00000260731.4:c.2106G>A ENSP00000260731.3:p.Lys702=
NM_004523.3:c.2106G>A NP_004514.2:p.Lys702=
NM_004523.4:c.2106G>A MANE Select NP_004514.2:p.Lys702=