Canonical Allele Identifier: CA1917600881

Gene: KIFBP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005056C= , CM000672.2:g.69005056C=	GRCh38
NC_000010.10:g.70764812C= , CM000672.1:g.70764812C=	GRCh37
NC_000010.9:g.70434818C=	NCBI36
NG_017061.1:g.21336C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.536C= MANE Select	ENSP00000354848.4:p.Pro179=
ENST00000625461.2:n.566C=
ENST00000626493.2:c.536C=	ENSP00000486692.1:p.Pro179=
ENST00000635779.2:c.536C=	ENSP00000489663.1:p.Pro179=
ENST00000635971.2:c.536C=	ENSP00000489878.2:p.Pro179=
ENST00000636200.2:c.536C=	ENSP00000490113.2:p.Pro179=
ENST00000637101.2:c.*109C=	ENSP00000490704.1:n.*109C=
ENST00000637104.2:c.*105C=	ENSP00000490019.2:n.*105C=
ENST00000637323.2:c.*177C=	ENSP00000489659.2:n.*177C=
ENST00000637420.2:c.536C=	ENSP00000490404.2:p.Pro179=
ENST00000637738.2:c.536C=	ENSP00000490742.2:p.Pro179=
ENST00000638119.2:c.611C=	ENSP00000490026.1:p.Pro204=
ENST00000674660.1:c.526-41C=	ENSP00000502562.1:n.526-41C=
ENST00000674688.1:n.566C=
ENST00000674897.1:c.20C=	ENSP00000502225.1:p.Pro7=
ENST00000674936.1:c.536C=	ENSP00000502484.1:p.Pro179=
ENST00000675576.1:c.437C=	ENSP00000502750.1:p.Pro146=
ENST00000676080.1:c.*49C=	ENSP00000502706.1:n.*49C=
ENST00000361983.6:c.536C=	ENSP00000354848.4:p.Pro179=
ENST00000625461.1:n.252C=
ENST00000626493.1:c.536C=	ENSP00000486692.1:p.Pro179=
NM_015634.3:c.536C=	NP_056449.1:p.Pro179=
NM_015634.4:c.536C= MANE Select	NP_056449.1:p.Pro179=