Canonical Allele Identifier: CA1153147235

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348580C= , CM000663.2:g.10348580C=	GRCh38
NC_000001.10:g.10408638C= , CM000663.1:g.10408638C=	GRCh37
NC_000001.9:g.10331225C=	NCBI36
NG_008069.1:g.142875C= , LRG_252:g.142875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3928-69C=	ENSP00000512668.1:n.3928-69C=
ENST00000696503.1:c.3790-69C=	ENSP00000512669.1:n.3790-69C=
ENST00000696504.1:c.3790-69C=	ENSP00000512670.1:n.3790-69C=
ENST00000676179.1:c.3865-69C= MANE Select	ENSP00000502065.1:n.3865-69C=
ENST00000263934.10:c.3727-69C=	ENSP00000263934.6:n.3727-69C=
ENST00000377081.5:c.3865-69C=	ENSP00000366284.1:n.3865-69C=
ENST00000377086.5:c.3865-69C=	ENSP00000366290.1:n.3865-69C=
ENST00000465635.5:n.320-69C=
ENST00000483340.1:n.401-69C=
ENST00000620295.2:c.3823-69C=	ENSP00000478500.1:n.3823-69C=
ENST00000622724.3:c.3787-69C=	ENSP00000480063.1:n.3787-69C=
NM_015074.3:c.3727-69C= , LRG_252t1:c.3727-69C=	NP_055889.2:n.3727-69C=
NM_001365951.1:c.3865-69C=	NP_001352880.1:n.3865-69C=
NM_001365952.1:c.3865-69C=	NP_001352881.1:n.3865-69C=
NM_001365951.3:c.3865-69C= MANE Select	NP_001352880.1:n.3865-69C=