Canonical Allele Identifier: CA470008534

Gene: KIFBP

Linked Data

• MyVariant Identifiers: chr10:g.70764834T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005078T>A , CM000672.2:g.69005078T>A	GRCh38
NC_000010.10:g.70764834T>A , CM000672.1:g.70764834T>A	GRCh37
NC_000010.9:g.70434840T>A	NCBI36
NG_017061.1:g.21358T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.558T>A MANE Select	ENSP00000354848.4:p.Arg186=
ENST00000625461.2:n.588T>A
ENST00000626493.2:c.558T>A	ENSP00000486692.1:p.Arg186=
ENST00000635779.2:c.558T>A	ENSP00000489663.1:p.Arg186=
ENST00000635971.2:c.558T>A	ENSP00000489878.2:p.Arg186=
ENST00000636200.2:c.558T>A	ENSP00000490113.2:p.Arg186=
ENST00000637101.2:c.*131T>A	ENSP00000490704.1:n.*131T>A
ENST00000637104.2:c.*127T>A	ENSP00000490019.2:n.*127T>A
ENST00000637323.2:c.*199T>A	ENSP00000489659.2:n.*199T>A
ENST00000637420.2:c.558T>A	ENSP00000490404.2:p.Arg186=
ENST00000637738.2:c.558T>A	ENSP00000490742.2:p.Arg186=
ENST00000638119.2:c.633T>A	ENSP00000490026.1:p.Arg211=
ENST00000674660.1:c.526-19T>A	ENSP00000502562.1:n.526-19T>A
ENST00000674688.1:n.588T>A
ENST00000674897.1:c.42T>A	ENSP00000502225.1:p.Arg14=
ENST00000674936.1:c.558T>A	ENSP00000502484.1:p.Arg186=
ENST00000675576.1:c.459T>A	ENSP00000502750.1:p.Arg153=
ENST00000676080.1:c.*71T>A	ENSP00000502706.1:n.*71T>A
ENST00000361983.6:c.558T>A	ENSP00000354848.4:p.Arg186=
ENST00000625461.1:n.274T>A
ENST00000626493.1:c.558T>A	ENSP00000486692.1:p.Arg186=
NM_015634.3:c.558T>A	NP_056449.1:p.Arg186=
NM_015634.4:c.558T>A MANE Select	NP_056449.1:p.Arg186=