Canonical Allele Identifier: CA1917600897

Gene: KIFBP

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69005085C= , CM000672.2:g.69005085C=	GRCh38
NC_000010.10:g.70764841C= , CM000672.1:g.70764841C=	GRCh37
NC_000010.9:g.70434847C=	NCBI36
NG_017061.1:g.21365C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361983.7:c.565C= MANE Select	ENSP00000354848.4:p.Pro189=
ENST00000625461.2:n.595C=
ENST00000626493.2:c.565C=	ENSP00000486692.1:p.Pro189=
ENST00000635779.2:c.565C=	ENSP00000489663.1:p.Pro189=
ENST00000635971.2:c.565C=	ENSP00000489878.2:p.Pro189=
ENST00000636200.2:c.565C=	ENSP00000490113.2:p.Pro189=
ENST00000637101.2:c.*138C=	ENSP00000490704.1:n.*138C=
ENST00000637104.2:c.*134C=	ENSP00000490019.2:n.*134C=
ENST00000637323.2:c.*206C=	ENSP00000489659.2:n.*206C=
ENST00000637420.2:c.565C=	ENSP00000490404.2:p.Pro189=
ENST00000637738.2:c.565C=	ENSP00000490742.2:p.Pro189=
ENST00000638119.2:c.640C=	ENSP00000490026.1:p.Pro214=
ENST00000674660.1:c.526-12C=	ENSP00000502562.1:n.526-12C=
ENST00000674688.1:n.595C=
ENST00000674897.1:c.49C=	ENSP00000502225.1:p.Pro17=
ENST00000674936.1:c.565C=	ENSP00000502484.1:p.Pro189=
ENST00000675576.1:c.466C=	ENSP00000502750.1:p.Pro156=
ENST00000676080.1:c.*78C=	ENSP00000502706.1:n.*78C=
ENST00000361983.6:c.565C=	ENSP00000354848.4:p.Pro189=
ENST00000625461.1:n.281C=
ENST00000626493.1:c.565C=	ENSP00000486692.1:p.Pro189=
NM_015634.3:c.565C=	NP_056449.1:p.Pro189=
NM_015634.4:c.565C= MANE Select	NP_056449.1:p.Pro189=