Canonical Allele Identifier: CA376896108
Gene: KIFBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005070A>T , CM000672.2:g.69005070A>T GRCh38
NC_000010.10:g.70764826A>T , CM000672.1:g.70764826A>T GRCh37
NC_000010.9:g.70434832A>T NCBI36
NG_017061.1:g.21350A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.550A>T MANE Select ENSP00000354848.4:p.Thr184Ser
ENST00000625461.2:n.580A>T
ENST00000626493.2:c.550A>T ENSP00000486692.1:p.Thr184Ser
ENST00000635779.2:c.550A>T ENSP00000489663.1:p.Thr184Ser
ENST00000635971.2:c.550A>T ENSP00000489878.2:p.Thr184Ser
ENST00000636200.2:c.550A>T ENSP00000490113.2:p.Thr184Ser
ENST00000637101.2:c.*123A>T ENSP00000490704.1:n.*123A>T
ENST00000637104.2:c.*119A>T ENSP00000490019.2:n.*119A>T
ENST00000637323.2:c.*191A>T ENSP00000489659.2:n.*191A>T
ENST00000637420.2:c.550A>T ENSP00000490404.2:p.Thr184Ser
ENST00000637738.2:c.550A>T ENSP00000490742.2:p.Thr184Ser
ENST00000638119.2:c.625A>T ENSP00000490026.1:p.Thr209Ser
ENST00000674660.1:c.526-27A>T ENSP00000502562.1:n.526-27A>T
ENST00000674688.1:n.580A>T
ENST00000674897.1:c.34A>T ENSP00000502225.1:p.Thr12Ser
ENST00000674936.1:c.550A>T ENSP00000502484.1:p.Thr184Ser
ENST00000675576.1:c.451A>T ENSP00000502750.1:p.Thr151Ser
ENST00000676080.1:c.*63A>T ENSP00000502706.1:n.*63A>T
ENST00000361983.6:c.550A>T ENSP00000354848.4:p.Thr184Ser
ENST00000625461.1:n.266A>T
ENST00000626493.1:c.550A>T ENSP00000486692.1:p.Thr184Ser
NM_015634.3:c.550A>T NP_056449.1:p.Thr184Ser
NM_015634.4:c.550A>T MANE Select NP_056449.1:p.Thr184Ser