Canonical Allele Identifier: CA1141580570

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345943C= , CM000663.2:g.10345943C=	GRCh38
NC_000001.10:g.10406001C= , CM000663.1:g.10406001C=	GRCh37
NC_000001.9:g.10328588C=	NCBI36
NG_008069.1:g.140238C= , LRG_252:g.140238C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3850C=	ENSP00000512668.1:p.Pro1284=
ENST00000696503.1:c.3712C=	ENSP00000512669.1:p.Pro1238=
ENST00000696504.1:c.3712C=	ENSP00000512670.1:p.Pro1238=
ENST00000676179.1:c.3787C= MANE Select	ENSP00000502065.1:p.Pro1263=
ENST00000263934.10:c.3649C=	ENSP00000263934.6:p.Pro1217=
ENST00000377081.5:c.3787C=	ENSP00000366284.1:p.Pro1263=
ENST00000377086.5:c.3787C=	ENSP00000366290.1:p.Pro1263=
ENST00000465635.5:n.242C=
ENST00000483340.1:n.323C=
ENST00000620295.2:c.3745C=	ENSP00000478500.1:p.Pro1249=
ENST00000622724.3:c.3709C=	ENSP00000480063.1:p.Pro1237=
NM_015074.3:c.3649C= , LRG_252t1:c.3649C=	NP_055889.2:p.Pro1217=
NM_001365951.1:c.3787C=	NP_001352880.1:p.Pro1263=
NM_001365952.1:c.3787C=	NP_001352881.1:p.Pro1263=
NM_001365951.3:c.3787C= MANE Select	NP_001352880.1:p.Pro1263=