Canonical Allele Identifier: CA1147430149

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345923T= , CM000663.2:g.10345923T=	GRCh38
NC_000001.10:g.10405981T= , CM000663.1:g.10405981T=	GRCh37
NC_000001.9:g.10328568T=	NCBI36
NG_008069.1:g.140218T= , LRG_252:g.140218T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3830T=	ENSP00000512668.1:p.Phe1277=
ENST00000696503.1:c.3692T=	ENSP00000512669.1:p.Phe1231=
ENST00000696504.1:c.3692T=	ENSP00000512670.1:p.Phe1231=
ENST00000676179.1:c.3767T= MANE Select	ENSP00000502065.1:p.Phe1256=
ENST00000263934.10:c.3629T=	ENSP00000263934.6:p.Phe1210=
ENST00000377081.5:c.3767T=	ENSP00000366284.1:p.Phe1256=
ENST00000377086.5:c.3767T=	ENSP00000366290.1:p.Phe1256=
ENST00000465635.5:n.222T=
ENST00000483340.1:n.303T=
ENST00000620295.2:c.3725T=	ENSP00000478500.1:p.Phe1242=
ENST00000622724.3:c.3689T=	ENSP00000480063.1:p.Phe1230=
NM_015074.3:c.3629T= , LRG_252t1:c.3629T=	NP_055889.2:p.Phe1210=
NM_001365951.1:c.3767T=	NP_001352880.1:p.Phe1256=
NM_001365952.1:c.3767T=	NP_001352881.1:p.Phe1256=
NM_001365951.3:c.3767T= MANE Select	NP_001352880.1:p.Phe1256=