Canonical Allele Identifier: CA1153146219

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345966T= , CM000663.2:g.10345966T=	GRCh38
NC_000001.10:g.10406024T= , CM000663.1:g.10406024T=	GRCh37
NC_000001.9:g.10328611T=	NCBI36
NG_008069.1:g.140261T= , LRG_252:g.140261T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3860+13T=	ENSP00000512668.1:n.3860+13T=
ENST00000696503.1:c.3722+13T=	ENSP00000512669.1:n.3722+13T=
ENST00000696504.1:c.3722+13T=	ENSP00000512670.1:n.3722+13T=
ENST00000676179.1:c.3797+13T= MANE Select	ENSP00000502065.1:n.3797+13T=
ENST00000263934.10:c.3659+13T=	ENSP00000263934.6:n.3659+13T=
ENST00000377081.5:c.3797+13T=	ENSP00000366284.1:n.3797+13T=
ENST00000377086.5:c.3797+13T=	ENSP00000366290.1:n.3797+13T=
ENST00000465635.5:n.252+13T=
ENST00000483340.1:n.333+13T=
ENST00000620295.2:c.3755+13T=	ENSP00000478500.1:n.3755+13T=
ENST00000622724.3:c.3719+13T=	ENSP00000480063.1:n.3719+13T=
NM_015074.3:c.3659+13T= , LRG_252t1:c.3659+13T=	NP_055889.2:n.3659+13T=
NM_001365951.1:c.3797+13T=	NP_001352880.1:n.3797+13T=
NM_001365952.1:c.3797+13T=	NP_001352881.1:n.3797+13T=
NM_001365951.3:c.3797+13T= MANE Select	NP_001352880.1:n.3797+13T=