Canonical Allele Identifier: CA338336816

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10326131G>A , CM000663.2:g.10326131G>A	GRCh38
NC_000001.10:g.10386189G>A , CM000663.1:g.10386189G>A	GRCh37
NC_000001.9:g.10308776G>A	NCBI36
NG_008069.1:g.120426G>A , LRG_252:g.120426G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.2696G>A MANE Select	NP_001352880.1:p.Cys899Tyr
ENST00000676179.1:c.2696G>A MANE Select	ENSP00000502065.1:p.Cys899Tyr
NM_001365951.1:c.2696G>A	NP_001352880.1:p.Cys899Tyr
NM_001365952.1:c.2696G>A	NP_001352881.1:p.Cys899Tyr
NM_015074.3:c.2558G>A , LRG_252t1:c.2558G>A	NP_055889.2:p.Cys853Tyr
ENST00000263934.10:c.2558G>A	ENSP00000263934.6:p.Cys853Tyr
ENST00000377081.5:c.2696G>A	ENSP00000366284.1:p.Cys899Tyr
ENST00000377086.5:c.2696G>A	ENSP00000366290.1:p.Cys899Tyr
ENST00000620295.2:c.2654G>A	ENSP00000478500.1:p.Cys885Tyr
ENST00000622724.3:c.2618G>A	ENSP00000480063.1:p.Cys873Tyr
ENST00000696502.1:c.2558G>A	ENSP00000512668.1:p.Cys853Tyr
ENST00000696503.1:c.2621G>A	ENSP00000512669.1:p.Cys874Tyr
ENST00000696504.1:c.2621G>A	ENSP00000512670.1:p.Cys874Tyr