Canonical Allele Identifier: CA1153159593

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324761G= , CM000663.2:g.10324761G=	GRCh38
NC_000001.10:g.10384819G= , CM000663.1:g.10384819G=	GRCh37
NC_000001.9:g.10307406G=	NCBI36
NG_008069.1:g.119056G= , LRG_252:g.119056G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.2403G=	ENSP00000512668.1:p.Gln801=
ENST00000696503.1:c.2466G=	ENSP00000512669.1:p.Gln822=
ENST00000696504.1:c.2466G=	ENSP00000512670.1:p.Gln822=
ENST00000676179.1:c.2541G= MANE Select	ENSP00000502065.1:p.Gln847=
ENST00000263934.10:c.2403G=	ENSP00000263934.6:p.Gln801=
ENST00000377081.5:c.2541G=	ENSP00000366284.1:p.Gln847=
ENST00000377086.5:c.2541G=	ENSP00000366290.1:p.Gln847=
ENST00000620295.2:c.2499G=	ENSP00000478500.1:p.Gln833=
ENST00000622724.3:c.2463G=	ENSP00000480063.1:p.Gln821=
NM_015074.3:c.2403G= , LRG_252t1:c.2403G=	NP_055889.2:p.Gln801=
NM_001365951.1:c.2541G=	NP_001352880.1:p.Gln847=
NM_001365952.1:c.2541G=	NP_001352881.1:p.Gln847=
NM_001365951.3:c.2541G= MANE Select	NP_001352880.1:p.Gln847=