Canonical Allele Identifier: CA206232
Gene: KIF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 211274
ClinVar RCV Id: RCV000193017
dbSNP Id: rs797045650
MyVariant Identifiers: chr10:g.94368825A>T (hg19) chr10:g.92609068A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.92609068A>T , CM000672.2:g.92609068A>T GRCh38
NC_000010.10:g.94368825A>T , CM000672.1:g.94368825A>T GRCh37
NC_000010.9:g.94358805A>T NCBI36
NG_032580.1:g.21001A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260731.5:c.436A>T MANE Select ENSP00000260731.3:p.Lys146Ter
ENST00000676621.1:c.436A>T ENSP00000503639.1:p.Lys146Ter
ENST00000676647.1:c.229A>T ENSP00000503394.1:p.Lys77Ter
ENST00000676757.1:c.229A>T ENSP00000504289.1:p.Lys77Ter
ENST00000677720.1:c.436A>T ENSP00000504840.1:p.Lys146Ter
ENST00000260731.4:c.436A>T ENSP00000260731.3:p.Lys146Ter
NM_004523.3:c.436A>T NP_004514.2:p.Lys146Ter
NM_004523.4:c.436A>T MANE Select NP_004514.2:p.Lys146Ter
Search 100 bp 5'
Search 100 bp 3'