Canonical Allele Identifier: CA376896161

Gene: KIFBP

Linked Data

• gnomAD v4: 10-69005082-C-G
• MyVariant Identifiers: chr10:g.70764838C>G (hg19) ; chr10:g.69005082C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.562C>G MANE Select	ENSP00000354848.4:p.Leu188Val
ENST00000625461.2:n.592C>G
ENST00000626493.2:c.562C>G	ENSP00000486692.1:p.Leu188Val
ENST00000635779.2:c.562C>G	ENSP00000489663.1:p.Leu188Val
ENST00000635971.2:c.562C>G	ENSP00000489878.2:p.Leu188Val
ENST00000636200.2:c.562C>G	ENSP00000490113.2:p.Leu188Val
ENST00000637101.2:c.*135C>G	ENSP00000490704.1:n.*135C>G
ENST00000637104.2:c.*131C>G	ENSP00000490019.2:n.*131C>G
ENST00000637323.2:c.*203C>G	ENSP00000489659.2:n.*203C>G
ENST00000637420.2:c.562C>G	ENSP00000490404.2:p.Leu188Val
ENST00000637738.2:c.562C>G	ENSP00000490742.2:p.Leu188Val
ENST00000638119.2:c.637C>G	ENSP00000490026.1:p.Leu213Val
ENST00000674660.1:c.526-15C>G	ENSP00000502562.1:n.526-15C>G
ENST00000674688.1:n.592C>G
ENST00000674897.1:c.46C>G	ENSP00000502225.1:p.Leu16Val
ENST00000674936.1:c.562C>G	ENSP00000502484.1:p.Leu188Val
ENST00000675576.1:c.463C>G	ENSP00000502750.1:p.Leu155Val
ENST00000676080.1:c.*75C>G	ENSP00000502706.1:n.*75C>G
ENST00000361983.6:c.562C>G	ENSP00000354848.4:p.Leu188Val
ENST00000625461.1:n.278C>G
ENST00000626493.1:c.562C>G	ENSP00000486692.1:p.Leu188Val
NM_015634.3:c.562C>G	NP_056449.1:p.Leu188Val
NM_015634.4:c.562C>G MANE Select	NP_056449.1:p.Leu188Val