Canonical Allele Identifier: CA1153146209
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10345916G= , CM000663.2:g.10345916G= GRCh38
NC_000001.10:g.10405974G= , CM000663.1:g.10405974G= GRCh37
NC_000001.9:g.10328561G= NCBI36
NG_008069.1:g.140211G= , LRG_252:g.140211G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3823G= ENSP00000512668.1:p.Val1275=
ENST00000696503.1:c.3685G= ENSP00000512669.1:p.Val1229=
ENST00000696504.1:c.3685G= ENSP00000512670.1:p.Val1229=
ENST00000676179.1:c.3760G= MANE Select ENSP00000502065.1:p.Val1254=
ENST00000263934.10:c.3622G= ENSP00000263934.6:p.Val1208=
ENST00000377081.5:c.3760G= ENSP00000366284.1:p.Val1254=
ENST00000377086.5:c.3760G= ENSP00000366290.1:p.Val1254=
ENST00000465635.5:n.215G=
ENST00000483340.1:n.296G=
ENST00000620295.2:c.3718G= ENSP00000478500.1:p.Val1240=
ENST00000622724.3:c.3682G= ENSP00000480063.1:p.Val1228=
NM_015074.3:c.3622G= , LRG_252t1:c.3622G= NP_055889.2:p.Val1208=
NM_001365951.1:c.3760G= NP_001352880.1:p.Val1254=
NM_001365952.1:c.3760G= NP_001352881.1:p.Val1254=
NM_001365951.3:c.3760G= MANE Select NP_001352880.1:p.Val1254=