Canonical Allele Identifier: CA2574206280
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10345860del , CM000663.2:g.10345860del GRCh38
NC_000001.10:g.10405918del , CM000663.1:g.10405918del GRCh37
NC_000001.9:g.10328505del NCBI36
NG_008069.1:g.140155del , LRG_252:g.140155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3767del ENSP00000512668.1:p.Leu1256Ter
ENST00000696503.1:c.3629del ENSP00000512669.1:p.Leu1210Ter
ENST00000696504.1:c.3629del ENSP00000512670.1:p.Leu1210Ter
ENST00000676179.1:c.3704del MANE Select ENSP00000502065.1:p.Leu1235Ter
ENST00000263934.10:c.3566del ENSP00000263934.6:p.Leu1189Ter
ENST00000377081.5:c.3704del ENSP00000366284.1:p.Leu1235Ter
ENST00000377086.5:c.3704del ENSP00000366290.1:p.Leu1235Ter
ENST00000465635.5:n.159del
ENST00000483340.1:n.240del
ENST00000620295.2:c.3662del ENSP00000478500.1:p.Leu1221Ter
ENST00000622724.3:c.3626del ENSP00000480063.1:p.Leu1209Ter
NM_015074.3:c.3566del , LRG_252t1:c.3566del NP_055889.2:p.Leu1189Ter
NM_001365951.1:c.3704del NP_001352880.1:p.Leu1235Ter
NM_001365952.1:c.3704del NP_001352881.1:p.Leu1235Ter
NM_001365951.3:c.3704del MANE Select NP_001352880.1:p.Leu1235Ter