Canonical Allele Identifier: CA415881643

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10384820A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324762A>C , CM000663.2:g.10324762A>C	GRCh38
NC_000001.10:g.10384820A>C , CM000663.1:g.10384820A>C	GRCh37
NC_000001.9:g.10307407A>C	NCBI36
NG_008069.1:g.119057A>C , LRG_252:g.119057A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.2404A>C	ENSP00000512668.1:p.Arg802=
ENST00000696503.1:c.2467A>C	ENSP00000512669.1:p.Arg823=
ENST00000696504.1:c.2467A>C	ENSP00000512670.1:p.Arg823=
ENST00000676179.1:c.2542A>C MANE Select	ENSP00000502065.1:p.Arg848=
ENST00000263934.10:c.2404A>C	ENSP00000263934.6:p.Arg802=
ENST00000377081.5:c.2542A>C	ENSP00000366284.1:p.Arg848=
ENST00000377086.5:c.2542A>C	ENSP00000366290.1:p.Arg848=
ENST00000620295.2:c.2500A>C	ENSP00000478500.1:p.Arg834=
ENST00000622724.3:c.2464A>C	ENSP00000480063.1:p.Arg822=
NM_015074.3:c.2404A>C , LRG_252t1:c.2404A>C	NP_055889.2:p.Arg802=
NM_001365951.1:c.2542A>C	NP_001352880.1:p.Arg848=
NM_001365952.1:c.2542A>C	NP_001352881.1:p.Arg848=
NM_001365951.3:c.2542A>C MANE Select	NP_001352880.1:p.Arg848=