Canonical Allele Identifier: CA209205885
Gene: KIFBP HGNC NCBI

Linked Data

dbSNP Id: rs112642097

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.550A>C MANE Select ENSP00000354848.4:p.Thr184Pro
ENST00000625461.2:n.580A>C
ENST00000626493.2:c.550A>C ENSP00000486692.1:p.Thr184Pro
ENST00000635779.2:c.550A>C ENSP00000489663.1:p.Thr184Pro
ENST00000635971.2:c.550A>C ENSP00000489878.2:p.Thr184Pro
ENST00000636200.2:c.550A>C ENSP00000490113.2:p.Thr184Pro
ENST00000637101.2:c.*123A>C ENSP00000490704.1:n.*123A>C
ENST00000637104.2:c.*119A>C ENSP00000490019.2:n.*119A>C
ENST00000637323.2:c.*191A>C ENSP00000489659.2:n.*191A>C
ENST00000637420.2:c.550A>C ENSP00000490404.2:p.Thr184Pro
ENST00000637738.2:c.550A>C ENSP00000490742.2:p.Thr184Pro
ENST00000638119.2:c.625A>C ENSP00000490026.1:p.Thr209Pro
ENST00000674660.1:c.526-27A>C ENSP00000502562.1:n.526-27A>C
ENST00000674688.1:n.580A>C
ENST00000674897.1:c.34A>C ENSP00000502225.1:p.Thr12Pro
ENST00000674936.1:c.550A>C ENSP00000502484.1:p.Thr184Pro
ENST00000675576.1:c.451A>C ENSP00000502750.1:p.Thr151Pro
ENST00000676080.1:c.*63A>C ENSP00000502706.1:n.*63A>C
ENST00000361983.6:c.550A>C ENSP00000354848.4:p.Thr184Pro
ENST00000625461.1:n.266A>C
ENST00000626493.1:c.550A>C ENSP00000486692.1:p.Thr184Pro
NM_015634.3:c.550A>C NP_056449.1:p.Thr184Pro
NM_015634.4:c.550A>C MANE Select NP_056449.1:p.Thr184Pro