Canonical Allele Identifier: CA1153161493

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365470C= , CM000663.2:g.10365470C=	GRCh38
NC_000001.10:g.10425528C= , CM000663.1:g.10425528C=	GRCh37
NC_000001.9:g.10348115C=	NCBI36
NG_008069.1:g.159765C= , LRG_252:g.159765C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4637C=	ENSP00000512668.1:p.Ser1546=
ENST00000696503.1:c.4499C=	ENSP00000512669.1:p.Ser1500=
ENST00000696504.1:c.4499C=	ENSP00000512670.1:p.Ser1500=
ENST00000676179.1:c.4574C= MANE Select	ENSP00000502065.1:p.Ser1525=
ENST00000263934.10:c.4436C=	ENSP00000263934.6:p.Ser1479=
ENST00000377081.5:c.4574C=	ENSP00000366284.1:p.Ser1525=
ENST00000377086.5:c.4574C=	ENSP00000366290.1:p.Ser1525=
ENST00000470616.1:n.305C=
ENST00000620295.2:c.4532C=	ENSP00000478500.1:p.Ser1511=
ENST00000622724.3:c.4496C=	ENSP00000480063.1:p.Ser1499=
ENST00000635499.1:c.619C=
NM_015074.3:c.4436C= , LRG_252t1:c.4436C=	NP_055889.2:p.Ser1479=
XR_946953.1:n.355+911G=
NM_001365951.1:c.4574C=	NP_001352880.1:p.Ser1525=
NM_001365952.1:c.4574C=	NP_001352881.1:p.Ser1525=
XR_946953.2:n.230+911G=
NM_001365951.3:c.4574C= MANE Select	NP_001352880.1:p.Ser1525=