Canonical Allele Identifier: CA582080

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365178G>A , CM000663.2:g.10365178G>A	GRCh38
NC_000001.10:g.10425236G>A , CM000663.1:g.10425236G>A	GRCh37
NC_000001.9:g.10347823G>A	NCBI36
NG_008069.1:g.159473G>A , LRG_252:g.159473G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4445G>A MANE Select	NP_001352880.1:p.Arg1482Gln
ENST00000676179.1:c.4445G>A MANE Select	ENSP00000502065.1:p.Arg1482Gln
NM_001365951.1:c.4445G>A	NP_001352880.1:p.Arg1482Gln
NM_001365952.1:c.4445G>A	NP_001352881.1:p.Arg1482Gln
NM_015074.3:c.4307G>A , LRG_252t1:c.4307G>A	NP_055889.2:p.Arg1436Gln
ENST00000263934.10:c.4307G>A	ENSP00000263934.6:p.Arg1436Gln
ENST00000377081.5:c.4445G>A	ENSP00000366284.1:p.Arg1482Gln
ENST00000377086.5:c.4445G>A	ENSP00000366290.1:p.Arg1482Gln
ENST00000470616.1:n.13G>A
ENST00000620295.2:c.4403G>A	ENSP00000478500.1:p.Arg1468Gln
ENST00000622724.3:c.4367G>A	ENSP00000480063.1:p.Arg1456Gln
ENST00000635499.1:c.490G>A
ENST00000696502.1:c.4508G>A	ENSP00000512668.1:p.Arg1503Gln
ENST00000696503.1:c.4370G>A	ENSP00000512669.1:p.Arg1457Gln
ENST00000696504.1:c.4370G>A	ENSP00000512670.1:p.Arg1457Gln
XR_946953.1:n.355+1203C>T
XR_946953.2:n.230+1203C>T