Canonical Allele Identifier: CA1153187091
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10343248C= , CM000663.2:g.10343248C= GRCh38
NC_000001.10:g.10403306C= , CM000663.1:g.10403306C= GRCh37
NC_000001.9:g.10325893C= NCBI36
NG_008069.1:g.137543C= , LRG_252:g.137543C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696502.1:c.3511C= ENSP00000512668.1:p.Arg1171=
ENST00000696503.1:c.3574C= ENSP00000512669.1:p.Arg1192=
ENST00000696504.1:c.3574C= ENSP00000512670.1:p.Arg1192=
ENST00000676179.1:c.3649C= MANE Select ENSP00000502065.1:p.Arg1217=
ENST00000263934.10:c.3511C= ENSP00000263934.6:p.Arg1171=
ENST00000377081.5:c.3649C= ENSP00000366284.1:p.Arg1217=
ENST00000377086.5:c.3649C= ENSP00000366290.1:p.Arg1217=
ENST00000620295.2:c.3607C= ENSP00000478500.1:p.Arg1203=
ENST00000622724.3:c.3571C= ENSP00000480063.1:p.Arg1191=
NM_015074.3:c.3511C= , LRG_252t1:c.3511C= NP_055889.2:p.Arg1171=
NM_001365951.1:c.3649C= NP_001352880.1:p.Arg1217=
NM_001365952.1:c.3649C= NP_001352881.1:p.Arg1217=
NM_001365951.3:c.3649C= MANE Select NP_001352880.1:p.Arg1217=