Canonical Allele Identifier: CA1917600895
Gene: KIFBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005082C= , CM000672.2:g.69005082C= GRCh38
NC_000010.10:g.70764838C= , CM000672.1:g.70764838C= GRCh37
NC_000010.9:g.70434844C= NCBI36
NG_017061.1:g.21362C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.562C= MANE Select ENSP00000354848.4:p.Leu188=
ENST00000625461.2:n.592C=
ENST00000626493.2:c.562C= ENSP00000486692.1:p.Leu188=
ENST00000635779.2:c.562C= ENSP00000489663.1:p.Leu188=
ENST00000635971.2:c.562C= ENSP00000489878.2:p.Leu188=
ENST00000636200.2:c.562C= ENSP00000490113.2:p.Leu188=
ENST00000637101.2:c.*135C= ENSP00000490704.1:n.*135C=
ENST00000637104.2:c.*131C= ENSP00000490019.2:n.*131C=
ENST00000637323.2:c.*203C= ENSP00000489659.2:n.*203C=
ENST00000637420.2:c.562C= ENSP00000490404.2:p.Leu188=
ENST00000637738.2:c.562C= ENSP00000490742.2:p.Leu188=
ENST00000638119.2:c.637C= ENSP00000490026.1:p.Leu213=
ENST00000674660.1:c.526-15C= ENSP00000502562.1:n.526-15C=
ENST00000674688.1:n.592C=
ENST00000674897.1:c.46C= ENSP00000502225.1:p.Leu16=
ENST00000674936.1:c.562C= ENSP00000502484.1:p.Leu188=
ENST00000675576.1:c.463C= ENSP00000502750.1:p.Leu155=
ENST00000676080.1:c.*75C= ENSP00000502706.1:n.*75C=
ENST00000361983.6:c.562C= ENSP00000354848.4:p.Leu188=
ENST00000625461.1:n.278C=
ENST00000626493.1:c.562C= ENSP00000486692.1:p.Leu188=
NM_015634.3:c.562C= NP_056449.1:p.Leu188=
NM_015634.4:c.562C= MANE Select NP_056449.1:p.Leu188=