Canonical Allele Identifier: CA376896342
Gene: KIFBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005117A>C , CM000672.2:g.69005117A>C GRCh38
NC_000010.10:g.70764873A>C , CM000672.1:g.70764873A>C GRCh37
NC_000010.9:g.70434879A>C NCBI36
NG_017061.1:g.21397A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.597A>C MANE Select ENSP00000354848.4:p.Arg199Ser
ENST00000625461.2:n.627A>C
ENST00000626493.2:c.597A>C ENSP00000486692.1:p.Arg199Ser
ENST00000635779.2:c.597A>C ENSP00000489663.1:p.Arg199Ser
ENST00000635971.2:c.597A>C ENSP00000489878.2:p.Arg199Ser
ENST00000636200.2:c.597A>C ENSP00000490113.2:p.Arg199Ser
ENST00000637101.2:c.*170A>C ENSP00000490704.1:n.*170A>C
ENST00000637104.2:c.*166A>C ENSP00000490019.2:n.*166A>C
ENST00000637323.2:c.*238A>C ENSP00000489659.2:n.*238A>C
ENST00000637420.2:c.597A>C ENSP00000490404.2:p.Arg199Ser
ENST00000637738.2:c.597A>C ENSP00000490742.2:p.Arg199Ser
ENST00000638119.2:c.672A>C ENSP00000490026.1:p.Arg224Ser
ENST00000674660.1:c.546A>C ENSP00000502562.1:p.Arg182Ser
ENST00000674688.1:n.627A>C
ENST00000674897.1:c.81A>C ENSP00000502225.1:p.Arg27Ser
ENST00000674936.1:c.597A>C ENSP00000502484.1:p.Arg199Ser
ENST00000675576.1:c.498A>C ENSP00000502750.1:p.Arg166Ser
ENST00000676080.1:c.*110A>C ENSP00000502706.1:n.*110A>C
ENST00000361983.6:c.597A>C ENSP00000354848.4:p.Arg199Ser
ENST00000625461.1:n.313A>C
ENST00000626493.1:c.597A>C ENSP00000486692.1:p.Arg199Ser
NM_015634.3:c.597A>C NP_056449.1:p.Arg199Ser
NM_015634.4:c.597A>C MANE Select NP_056449.1:p.Arg199Ser