Canonical Allele Identifier: CA376896017
Gene: KIFBP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361983.7:c.526G>C MANE Select ENSP00000354848.4:p.Val176Leu
ENST00000625461.2:n.556G>C
ENST00000626493.2:c.526G>C ENSP00000486692.1:p.Val176Leu
ENST00000635779.2:c.526G>C ENSP00000489663.1:p.Val176Leu
ENST00000635971.2:c.526G>C ENSP00000489878.2:p.Val176Leu
ENST00000636200.2:c.526G>C ENSP00000490113.2:p.Val176Leu
ENST00000637101.2:c.*99G>C ENSP00000490704.1:n.*99G>C
ENST00000637104.2:c.*95G>C ENSP00000490019.2:n.*95G>C
ENST00000637323.2:c.*167G>C ENSP00000489659.2:n.*167G>C
ENST00000637420.2:c.526G>C ENSP00000490404.2:p.Val176Leu
ENST00000637738.2:c.526G>C ENSP00000490742.2:p.Val176Leu
ENST00000638119.2:c.601G>C ENSP00000490026.1:p.Val201Leu
ENST00000674660.1:c.526-51G>C ENSP00000502562.1:n.526-51G>C
ENST00000674688.1:n.556G>C
ENST00000674897.1:c.10G>C ENSP00000502225.1:p.Val4Leu
ENST00000674936.1:c.526G>C ENSP00000502484.1:p.Val176Leu
ENST00000675576.1:c.427G>C ENSP00000502750.1:p.Val143Leu
ENST00000676080.1:c.*39G>C ENSP00000502706.1:n.*39G>C
ENST00000361983.6:c.526G>C ENSP00000354848.4:p.Val176Leu
ENST00000625461.1:n.242G>C
ENST00000626493.1:c.526G>C ENSP00000486692.1:p.Val176Leu
NM_015634.3:c.526G>C NP_056449.1:p.Val176Leu
NM_015634.4:c.526G>C MANE Select NP_056449.1:p.Val176Leu