Canonical Allele Identifier: CA1153159676
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10324787A= , CM000663.2:g.10324787A= GRCh38
NC_000001.10:g.10384845A= , CM000663.1:g.10384845A= GRCh37
NC_000001.9:g.10307432A= NCBI36
NG_008069.1:g.119082A= , LRG_252:g.119082A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.2429A= ENSP00000512668.1:p.Tyr810=
ENST00000696503.1:c.2492A= ENSP00000512669.1:p.Tyr831=
ENST00000696504.1:c.2492A= ENSP00000512670.1:p.Tyr831=
ENST00000676179.1:c.2567A= MANE Select ENSP00000502065.1:p.Tyr856=
ENST00000263934.10:c.2429A= ENSP00000263934.6:p.Tyr810=
ENST00000377081.5:c.2567A= ENSP00000366284.1:p.Tyr856=
ENST00000377086.5:c.2567A= ENSP00000366290.1:p.Tyr856=
ENST00000620295.2:c.2525A= ENSP00000478500.1:p.Tyr842=
ENST00000622724.3:c.2489A= ENSP00000480063.1:p.Tyr830=
NM_015074.3:c.2429A= , LRG_252t1:c.2429A= NP_055889.2:p.Tyr810=
NM_001365951.1:c.2567A= NP_001352880.1:p.Tyr856=
NM_001365952.1:c.2567A= NP_001352881.1:p.Tyr856=
NM_001365951.3:c.2567A= MANE Select NP_001352880.1:p.Tyr856=