Canonical Allele Identifier: CA251940
Gene: KIFBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1733
ClinVar RCV Id: RCV001794428
dbSNP Id: rs121434514
MyVariant Identifiers: chr10:g.70748856C>T (hg19) chr10:g.68989100C>T (hg38)
PubMed: PMID:15883926 PMID:23427148
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68989100C>T , CM000672.2:g.68989100C>T GRCh38
NC_000010.10:g.70748856C>T , CM000672.1:g.70748856C>T GRCh37
NC_000010.9:g.70418862C>T NCBI36
NG_017061.1:g.5380C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361983.7:c.268C>T MANE Select ENSP00000354848.4:p.Arg90Ter
ENST00000625461.2:n.298C>T
ENST00000626493.2:c.268C>T ENSP00000486692.1:p.Arg90Ter
ENST00000635779.2:c.268C>T ENSP00000489663.1:p.Arg90Ter
ENST00000635971.2:c.268C>T ENSP00000489878.2:p.Arg90Ter
ENST00000636200.2:c.268C>T ENSP00000490113.2:p.Arg90Ter
ENST00000637101.2:c.268C>T ENSP00000490704.1:p.Arg90Ter
ENST00000637104.2:c.268C>T ENSP00000490019.2:p.Arg90Ter
ENST00000637323.2:c.268C>T ENSP00000489659.2:p.Arg90Ter
ENST00000637420.2:c.268C>T ENSP00000490404.2:p.Arg90Ter
ENST00000637738.2:c.268C>T ENSP00000490742.2:p.Arg90Ter
ENST00000638119.2:c.268C>T ENSP00000490026.1:p.Arg90Ter
ENST00000674660.1:c.268C>T ENSP00000502562.1:p.Arg90Ter
ENST00000674688.1:n.298C>T
ENST00000674936.1:c.268C>T ENSP00000502484.1:p.Arg90Ter
ENST00000675576.1:c.268C>T ENSP00000502750.1:p.Arg90Ter
ENST00000676080.1:c.268C>T ENSP00000502706.1:p.Arg90Ter
ENST00000361983.6:c.268C>T ENSP00000354848.4:p.Arg90Ter
ENST00000626493.1:c.268C>T ENSP00000486692.1:p.Arg90Ter
NM_015634.3:c.268C>T NP_056449.1:p.Arg90Ter
NM_015634.4:c.268C>T MANE Select NP_056449.1:p.Arg90Ter
Search 100 bp 5'
Search 100 bp 3'