Canonical Allele Identifier: CA1153199093

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368475A= , CM000663.2:g.10368475A=	GRCh38
NC_000001.10:g.10428533A= , CM000663.1:g.10428533A=	GRCh37
NC_000001.9:g.10351120A=	NCBI36
NG_008069.1:g.162770A= , LRG_252:g.162770A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4824A=	ENSP00000512668.1:p.Gln1608=
ENST00000696503.1:c.4686A=	ENSP00000512669.1:p.Gln1562=
ENST00000696504.1:c.4686A=	ENSP00000512670.1:p.Gln1562=
ENST00000676179.1:c.4761A= MANE Select	ENSP00000502065.1:p.Gln1587=
ENST00000263934.10:c.4623A=	ENSP00000263934.6:p.Gln1541=
ENST00000377081.5:c.4761A=	ENSP00000366284.1:p.Gln1587=
ENST00000377086.5:c.4761A=	ENSP00000366290.1:p.Gln1587=
ENST00000470616.1:n.492A=
ENST00000620295.2:c.4719A=	ENSP00000478500.1:p.Gln1573=
ENST00000622724.3:c.4683A=	ENSP00000480063.1:p.Gln1561=
ENST00000635499.1:c.806A=
NM_015074.3:c.4623A= , LRG_252t1:c.4623A=	NP_055889.2:p.Gln1541=
NM_001365951.1:c.4761A=	NP_001352880.1:p.Gln1587=
NM_001365952.1:c.4761A=	NP_001352881.1:p.Gln1587=
NM_001365951.3:c.4761A= MANE Select	NP_001352880.1:p.Gln1587=