Canonical Allele Identifier: CA377594322

Gene: KIF11

Linked Data

• gnomAD v4: 10-92645571-A-G
• MyVariant Identifiers: chr10:g.94405328A>G (hg19) ; chr10:g.92645571A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92645571A>G , CM000672.2:g.92645571A>G	GRCh38
NC_000010.10:g.94405328A>G , CM000672.1:g.94405328A>G	GRCh37
NC_000010.9:g.94395308A>G	NCBI36
NG_032580.1:g.57504A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260731.5:c.2476A>G MANE Select	ENSP00000260731.3:p.Thr826Ala
ENST00000676621.1:c.*994A>G	ENSP00000503639.1:n.*994A>G
ENST00000676647.1:c.2269A>G	ENSP00000503394.1:p.Thr757Ala
ENST00000676757.1:c.2269A>G	ENSP00000504289.1:p.Thr757Ala
ENST00000677720.1:c.*450A>G	ENSP00000504840.1:n.*450A>G
ENST00000260731.4:c.2476A>G	ENSP00000260731.3:p.Thr826Ala
NM_004523.3:c.2476A>G	NP_004514.2:p.Thr826Ala
NM_004523.4:c.2476A>G MANE Select	NP_004514.2:p.Thr826Ala