Canonical Allele Identifier: CA1917600877
Gene: KIFBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005046G= , CM000672.2:g.69005046G= GRCh38
NC_000010.10:g.70764802G= , CM000672.1:g.70764802G= GRCh37
NC_000010.9:g.70434808G= NCBI36
NG_017061.1:g.21326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.526G= MANE Select ENSP00000354848.4:p.Val176=
ENST00000625461.2:n.556G=
ENST00000626493.2:c.526G= ENSP00000486692.1:p.Val176=
ENST00000635779.2:c.526G= ENSP00000489663.1:p.Val176=
ENST00000635971.2:c.526G= ENSP00000489878.2:p.Val176=
ENST00000636200.2:c.526G= ENSP00000490113.2:p.Val176=
ENST00000637101.2:c.*99G= ENSP00000490704.1:n.*99G=
ENST00000637104.2:c.*95G= ENSP00000490019.2:n.*95G=
ENST00000637323.2:c.*167G= ENSP00000489659.2:n.*167G=
ENST00000637420.2:c.526G= ENSP00000490404.2:p.Val176=
ENST00000637738.2:c.526G= ENSP00000490742.2:p.Val176=
ENST00000638119.2:c.601G= ENSP00000490026.1:p.Val201=
ENST00000674660.1:c.526-51G= ENSP00000502562.1:n.526-51G=
ENST00000674688.1:n.556G=
ENST00000674897.1:c.10G= ENSP00000502225.1:p.Val4=
ENST00000674936.1:c.526G= ENSP00000502484.1:p.Val176=
ENST00000675576.1:c.427G= ENSP00000502750.1:p.Val143=
ENST00000676080.1:c.*39G= ENSP00000502706.1:n.*39G=
ENST00000361983.6:c.526G= ENSP00000354848.4:p.Val176=
ENST00000625461.1:n.242G=
ENST00000626493.1:c.526G= ENSP00000486692.1:p.Val176=
NM_015634.3:c.526G= NP_056449.1:p.Val176=
NM_015634.4:c.526G= MANE Select NP_056449.1:p.Val176=