Canonical Allele Identifier: CA2574206203
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10343320C>G , CM000663.2:g.10343320C>G GRCh38
NC_000001.10:g.10403378C>G , CM000663.1:g.10403378C>G GRCh37
NC_000001.9:g.10325965C>G NCBI36
NG_008069.1:g.137615C>G , LRG_252:g.137615C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3550+33C>G ENSP00000512668.1:n.3550+33C>G
ENST00000696503.1:c.3613+33C>G ENSP00000512669.1:n.3613+33C>G
ENST00000696504.1:c.3613+33C>G ENSP00000512670.1:n.3613+33C>G
ENST00000676179.1:c.3688+33C>G MANE Select ENSP00000502065.1:n.3688+33C>G
ENST00000263934.10:c.3550+33C>G ENSP00000263934.6:n.3550+33C>G
ENST00000377081.5:c.3688+33C>G ENSP00000366284.1:n.3688+33C>G
ENST00000377086.5:c.3688+33C>G ENSP00000366290.1:n.3688+33C>G
ENST00000620295.2:c.3646+33C>G ENSP00000478500.1:n.3646+33C>G
ENST00000622724.3:c.3610+33C>G ENSP00000480063.1:n.3610+33C>G
NM_015074.3:c.3550+33C>G , LRG_252t1:c.3550+33C>G NP_055889.2:n.3550+33C>G
NM_001365951.1:c.3688+33C>G NP_001352880.1:n.3688+33C>G
NM_001365952.1:c.3688+33C>G NP_001352881.1:n.3688+33C>G
NM_001365951.3:c.3688+33C>G MANE Select NP_001352880.1:n.3688+33C>G