Canonical Allele Identifier: CA376896103

Gene: KIFBP

Linked Data

• MyVariant Identifiers: chr10:g.70764824C>G (hg19) ; chr10:g.69005068C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005068C>G , CM000672.2:g.69005068C>G	GRCh38
NC_000010.10:g.70764824C>G , CM000672.1:g.70764824C>G	GRCh37
NC_000010.9:g.70434830C>G	NCBI36
NG_017061.1:g.21348C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.548C>G MANE Select	ENSP00000354848.4:p.Pro183Arg
ENST00000625461.2:n.578C>G
ENST00000626493.2:c.548C>G	ENSP00000486692.1:p.Pro183Arg
ENST00000635779.2:c.548C>G	ENSP00000489663.1:p.Pro183Arg
ENST00000635971.2:c.548C>G	ENSP00000489878.2:p.Pro183Arg
ENST00000636200.2:c.548C>G	ENSP00000490113.2:p.Pro183Arg
ENST00000637101.2:c.*121C>G	ENSP00000490704.1:n.*121C>G
ENST00000637104.2:c.*117C>G	ENSP00000490019.2:n.*117C>G
ENST00000637323.2:c.*189C>G	ENSP00000489659.2:n.*189C>G
ENST00000637420.2:c.548C>G	ENSP00000490404.2:p.Pro183Arg
ENST00000637738.2:c.548C>G	ENSP00000490742.2:p.Pro183Arg
ENST00000638119.2:c.623C>G	ENSP00000490026.1:p.Pro208Arg
ENST00000674660.1:c.526-29C>G	ENSP00000502562.1:n.526-29C>G
ENST00000674688.1:n.578C>G
ENST00000674897.1:c.32C>G	ENSP00000502225.1:p.Pro11Arg
ENST00000674936.1:c.548C>G	ENSP00000502484.1:p.Pro183Arg
ENST00000675576.1:c.449C>G	ENSP00000502750.1:p.Pro150Arg
ENST00000676080.1:c.*61C>G	ENSP00000502706.1:n.*61C>G
ENST00000361983.6:c.548C>G	ENSP00000354848.4:p.Pro183Arg
ENST00000625461.1:n.264C>G
ENST00000626493.1:c.548C>G	ENSP00000486692.1:p.Pro183Arg
NM_015634.3:c.548C>G	NP_056449.1:p.Pro183Arg
NM_015634.4:c.548C>G MANE Select	NP_056449.1:p.Pro183Arg