Canonical Allele Identifier: CA1153146212

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345931A= , CM000663.2:g.10345931A=	GRCh38
NC_000001.10:g.10405989A= , CM000663.1:g.10405989A=	GRCh37
NC_000001.9:g.10328576A=	NCBI36
NG_008069.1:g.140226A= , LRG_252:g.140226A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3838A=	ENSP00000512668.1:p.Ser1280=
ENST00000696503.1:c.3700A=	ENSP00000512669.1:p.Ser1234=
ENST00000696504.1:c.3700A=	ENSP00000512670.1:p.Ser1234=
ENST00000676179.1:c.3775A= MANE Select	ENSP00000502065.1:p.Ser1259=
ENST00000263934.10:c.3637A=	ENSP00000263934.6:p.Ser1213=
ENST00000377081.5:c.3775A=	ENSP00000366284.1:p.Ser1259=
ENST00000377086.5:c.3775A=	ENSP00000366290.1:p.Ser1259=
ENST00000465635.5:n.230A=
ENST00000483340.1:n.311A=
ENST00000620295.2:c.3733A=	ENSP00000478500.1:p.Ser1245=
ENST00000622724.3:c.3697A=	ENSP00000480063.1:p.Ser1233=
NM_015074.3:c.3637A= , LRG_252t1:c.3637A=	NP_055889.2:p.Ser1213=
NM_001365951.1:c.3775A=	NP_001352880.1:p.Ser1259=
NM_001365952.1:c.3775A=	NP_001352881.1:p.Ser1259=
NM_001365951.3:c.3775A= MANE Select	NP_001352880.1:p.Ser1259=