Canonical Allele Identifier: CA1153199096

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368485C= , CM000663.2:g.10368485C=	GRCh38
NC_000001.10:g.10428543C= , CM000663.1:g.10428543C=	GRCh37
NC_000001.9:g.10351130C=	NCBI36
NG_008069.1:g.162780C= , LRG_252:g.162780C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.4834C=	ENSP00000512668.1:p.His1612=
ENST00000696503.1:c.4696C=	ENSP00000512669.1:p.His1566=
ENST00000696504.1:c.4696C=	ENSP00000512670.1:p.His1566=
ENST00000676179.1:c.4771C= MANE Select	ENSP00000502065.1:p.His1591=
ENST00000263934.10:c.4633C=	ENSP00000263934.6:p.His1545=
ENST00000377081.5:c.4771C=	ENSP00000366284.1:p.His1591=
ENST00000377086.5:c.4771C=	ENSP00000366290.1:p.His1591=
ENST00000470616.1:n.502C=
ENST00000620295.2:c.4729C=	ENSP00000478500.1:p.His1577=
ENST00000622724.3:c.4693C=	ENSP00000480063.1:p.His1565=
ENST00000635499.1:c.816C=
NM_015074.3:c.4633C= , LRG_252t1:c.4633C=	NP_055889.2:p.His1545=
NM_001365951.1:c.4771C=	NP_001352880.1:p.His1591=
NM_001365952.1:c.4771C=	NP_001352881.1:p.His1591=
NM_001365951.3:c.4771C= MANE Select	NP_001352880.1:p.His1591=