Canonical Allele Identifier: CA338335827
Gene: KIF1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10324882A>C , CM000663.2:g.10324882A>C GRCh38
NC_000001.10:g.10384940A>C , CM000663.1:g.10384940A>C GRCh37
NC_000001.9:g.10307527A>C NCBI36
NG_008069.1:g.119177A>C , LRG_252:g.119177A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.2524A>C ENSP00000512668.1:p.Lys842Gln
ENST00000696503.1:c.2587A>C ENSP00000512669.1:p.Lys863Gln
ENST00000696504.1:c.2587A>C ENSP00000512670.1:p.Lys863Gln
ENST00000676179.1:c.2662A>C MANE Select ENSP00000502065.1:p.Lys888Gln
ENST00000263934.10:c.2524A>C ENSP00000263934.6:p.Lys842Gln
ENST00000377081.5:c.2662A>C ENSP00000366284.1:p.Lys888Gln
ENST00000377086.5:c.2662A>C ENSP00000366290.1:p.Lys888Gln
ENST00000620295.2:c.2620A>C ENSP00000478500.1:p.Lys874Gln
ENST00000622724.3:c.2584A>C ENSP00000480063.1:p.Lys862Gln
NM_015074.3:c.2524A>C , LRG_252t1:c.2524A>C NP_055889.2:p.Lys842Gln
NM_001365951.1:c.2662A>C NP_001352880.1:p.Lys888Gln
NM_001365952.1:c.2662A>C NP_001352881.1:p.Lys888Gln
NM_001365951.3:c.2662A>C MANE Select NP_001352880.1:p.Lys888Gln