Canonical Allele Identifier: CA1153149491
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10296591C= , CM000663.2:g.10296591C= GRCh38
NC_000001.10:g.10356649C= , CM000663.1:g.10356649C= GRCh37
NC_000001.9:g.10279236C= NCBI36
NG_008069.1:g.90886C= , LRG_252:g.90886C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696500.1:c.*821C= ENSP00000512666.1:n.*821C=
ENST00000696502.1:c.1649C= ENSP00000512668.1:p.Thr550=
ENST00000696503.1:c.1712C= ENSP00000512669.1:p.Thr571=
ENST00000696504.1:c.1712C= ENSP00000512670.1:p.Thr571=
ENST00000377093.9:c.1649C= ENSP00000366297.4:p.Thr550=
ENST00000676179.1:c.1787C= MANE Select ENSP00000502065.1:p.Thr596=
ENST00000263934.10:c.1649C= ENSP00000263934.6:p.Thr550=
ENST00000377081.5:c.1787C= ENSP00000366284.1:p.Thr596=
ENST00000377083.5:c.1649C= ENSP00000366287.1:p.Thr550=
ENST00000377086.5:c.1787C= ENSP00000366290.1:p.Thr596=
ENST00000377093.8:c.1649C= ENSP00000366297.4:p.Thr550=
ENST00000620295.2:c.1745C= ENSP00000478500.1:p.Thr582=
ENST00000622724.3:c.1709C= ENSP00000480063.1:p.Thr570=
NM_015074.3:c.1649C= , LRG_252t1:c.1649C= NP_055889.2:p.Thr550=
NM_183416.3:c.1649C= NP_904325.2:p.Thr550=
NM_001365951.1:c.1787C= NP_001352880.1:p.Thr596=
NM_001365952.1:c.1787C= NP_001352881.1:p.Thr596=
NM_001365953.1:c.1649C= NP_001352882.1:p.Thr550=
NM_001365951.3:c.1787C= MANE Select NP_001352880.1:p.Thr596=
NM_183416.4:c.1649C= NP_904325.2:p.Thr550=