Canonical Allele Identifier: CA1140468477
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10226118G= , CM000663.2:g.10226118G= GRCh38
NC_000001.10:g.10286176G= , CM000663.1:g.10286176G= GRCh37
NC_000001.9:g.10208763G= NCBI36
NG_008069.1:g.20413G= , LRG_252:g.20413G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696500.1:c.-79-6132G= ENSP00000512666.1:n.-79-6132G=
ENST00000696501.1:c.-79-6132G= ENSP00000512667.1:n.-79-6132G=
ENST00000696502.1:c.-79-6132G= ENSP00000512668.1:n.-79-6132G=
ENST00000696503.1:c.-79-6132G= ENSP00000512669.1:n.-79-6132G=
ENST00000696504.1:c.-79-6132G= ENSP00000512670.1:n.-79-6132G=
ENST00000377093.9:c.-79-6132G= ENSP00000366297.4:n.-79-6132G=
ENST00000676179.1:c.-79-6132G= MANE Select ENSP00000502065.1:n.-79-6132G=
ENST00000263934.10:c.-79-6132G= ENSP00000263934.6:n.-79-6132G=
ENST00000377086.5:c.-79-6132G= ENSP00000366290.1:n.-79-6132G=
ENST00000377093.8:c.-79-6132G= ENSP00000366297.4:n.-79-6132G=
NM_015074.3:c.-79-6132G= , LRG_252t1:c.-79-6132G= NP_055889.2:n.-79-6132G=
NM_183416.3:c.-79-6132G= NP_904325.2:n.-79-6132G=
NM_001365951.1:c.-79-6132G= NP_001352880.1:n.-79-6132G=
NM_001365952.1:c.-79-6132G= NP_001352881.1:n.-79-6132G=
NM_001365951.3:c.-79-6132G= MANE Select NP_001352880.1:n.-79-6132G=
NM_183416.4:c.-79-6132G= NP_904325.2:n.-79-6132G=