Canonical Allele Identifier: CA1147127756

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348587C= , CM000663.2:g.10348587C=	GRCh38
NC_000001.10:g.10408645C= , CM000663.1:g.10408645C=	GRCh37
NC_000001.9:g.10331232C=	NCBI36
NG_008069.1:g.142882C= , LRG_252:g.142882C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.3928-62C=	ENSP00000512668.1:n.3928-62C=
ENST00000696503.1:c.3790-62C=	ENSP00000512669.1:n.3790-62C=
ENST00000696504.1:c.3790-62C=	ENSP00000512670.1:n.3790-62C=
ENST00000676179.1:c.3865-62C= MANE Select	ENSP00000502065.1:n.3865-62C=
ENST00000263934.10:c.3727-62C=	ENSP00000263934.6:n.3727-62C=
ENST00000377081.5:c.3865-62C=	ENSP00000366284.1:n.3865-62C=
ENST00000377086.5:c.3865-62C=	ENSP00000366290.1:n.3865-62C=
ENST00000465635.5:n.320-62C=
ENST00000483340.1:n.401-62C=
ENST00000620295.2:c.3823-62C=	ENSP00000478500.1:n.3823-62C=
ENST00000622724.3:c.3787-62C=	ENSP00000480063.1:n.3787-62C=
NM_015074.3:c.3727-62C= , LRG_252t1:c.3727-62C=	NP_055889.2:n.3727-62C=
NM_001365951.1:c.3865-62C=	NP_001352880.1:n.3865-62C=
NM_001365952.1:c.3865-62C=	NP_001352881.1:n.3865-62C=
NM_001365951.3:c.3865-62C= MANE Select	NP_001352880.1:n.3865-62C=