Canonical Allele Identifier: CA376896130
Gene: KIFBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69005075G>C , CM000672.2:g.69005075G>C GRCh38
NC_000010.10:g.70764831G>C , CM000672.1:g.70764831G>C GRCh37
NC_000010.9:g.70434837G>C NCBI36
NG_017061.1:g.21355G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.555G>C MANE Select ENSP00000354848.4:p.Glu185Asp
ENST00000625461.2:n.585G>C
ENST00000626493.2:c.555G>C ENSP00000486692.1:p.Glu185Asp
ENST00000635779.2:c.555G>C ENSP00000489663.1:p.Glu185Asp
ENST00000635971.2:c.555G>C ENSP00000489878.2:p.Glu185Asp
ENST00000636200.2:c.555G>C ENSP00000490113.2:p.Glu185Asp
ENST00000637101.2:c.*128G>C ENSP00000490704.1:n.*128G>C
ENST00000637104.2:c.*124G>C ENSP00000490019.2:n.*124G>C
ENST00000637323.2:c.*196G>C ENSP00000489659.2:n.*196G>C
ENST00000637420.2:c.555G>C ENSP00000490404.2:p.Glu185Asp
ENST00000637738.2:c.555G>C ENSP00000490742.2:p.Glu185Asp
ENST00000638119.2:c.630G>C ENSP00000490026.1:p.Glu210Asp
ENST00000674660.1:c.526-22G>C ENSP00000502562.1:n.526-22G>C
ENST00000674688.1:n.585G>C
ENST00000674897.1:c.39G>C ENSP00000502225.1:p.Glu13Asp
ENST00000674936.1:c.555G>C ENSP00000502484.1:p.Glu185Asp
ENST00000675576.1:c.456G>C ENSP00000502750.1:p.Glu152Asp
ENST00000676080.1:c.*68G>C ENSP00000502706.1:n.*68G>C
ENST00000361983.6:c.555G>C ENSP00000354848.4:p.Glu185Asp
ENST00000625461.1:n.271G>C
ENST00000626493.1:c.555G>C ENSP00000486692.1:p.Glu185Asp
NM_015634.3:c.555G>C NP_056449.1:p.Glu185Asp
NM_015634.4:c.555G>C MANE Select NP_056449.1:p.Glu185Asp