Canonical Allele Identifier: CA376896344
Gene: KIFBP HGNC NCBI

Linked Data

dbSNP Id: rs1843517955

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005118T>A , CM000672.2:g.69005118T>A GRCh38
NC_000010.10:g.70764874T>A , CM000672.1:g.70764874T>A GRCh37
NC_000010.9:g.70434880T>A NCBI36
NG_017061.1:g.21398T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.598T>A MANE Select ENSP00000354848.4:p.Ser200Thr
ENST00000625461.2:n.628T>A
ENST00000626493.2:c.598T>A ENSP00000486692.1:p.Ser200Thr
ENST00000635779.2:c.598T>A ENSP00000489663.1:p.Ser200Thr
ENST00000635971.2:c.598T>A ENSP00000489878.2:p.Ser200Thr
ENST00000636200.2:c.598T>A ENSP00000490113.2:p.Ser200Thr
ENST00000637101.2:c.*171T>A ENSP00000490704.1:n.*171T>A
ENST00000637104.2:c.*167T>A ENSP00000490019.2:n.*167T>A
ENST00000637323.2:c.*239T>A ENSP00000489659.2:n.*239T>A
ENST00000637420.2:c.598T>A ENSP00000490404.2:p.Ser200Thr
ENST00000637738.2:c.598T>A ENSP00000490742.2:p.Ser200Thr
ENST00000638119.2:c.673T>A ENSP00000490026.1:p.Ser225Thr
ENST00000674660.1:c.547T>A ENSP00000502562.1:p.Ser183Thr
ENST00000674688.1:n.628T>A
ENST00000674897.1:c.82T>A ENSP00000502225.1:p.Ser28Thr
ENST00000674936.1:c.598T>A ENSP00000502484.1:p.Ser200Thr
ENST00000675576.1:c.499T>A ENSP00000502750.1:p.Ser167Thr
ENST00000676080.1:c.*111T>A ENSP00000502706.1:n.*111T>A
ENST00000361983.6:c.598T>A ENSP00000354848.4:p.Ser200Thr
ENST00000625461.1:n.314T>A
ENST00000626493.1:c.598T>A ENSP00000486692.1:p.Ser200Thr
NM_015634.3:c.598T>A NP_056449.1:p.Ser200Thr
NM_015634.4:c.598T>A MANE Select NP_056449.1:p.Ser200Thr