Canonical Allele Identifier: CA581995
Gene: KIF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 284219
dbSNP Id: rs116302604
gnomAD v2: 1-10421089-G-A
gnomAD v3: 1-10361031-G-A
gnomAD v4: 1-10361031-G-A
COSMIC: COSM245284

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10361031G>A , CM000663.2:g.10361031G>A GRCh38
NC_000001.10:g.10421089G>A , CM000663.1:g.10421089G>A GRCh37
NC_000001.9:g.10343676G>A NCBI36
NG_008069.1:g.155326G>A , LRG_252:g.155326G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696502.1:c.4221G>A ENSP00000512668.1:p.Ser1407=
ENST00000696503.1:c.4083G>A ENSP00000512669.1:p.Ser1361=
ENST00000696504.1:c.4083G>A ENSP00000512670.1:p.Ser1361=
ENST00000676179.1:c.4158G>A MANE Select ENSP00000502065.1:p.Ser1386=
ENST00000263934.10:c.4020G>A ENSP00000263934.6:p.Ser1340=
ENST00000377081.5:c.4158G>A ENSP00000366284.1:p.Ser1386=
ENST00000377086.5:c.4158G>A ENSP00000366290.1:p.Ser1386=
ENST00000465635.5:n.613G>A
ENST00000483340.1:n.694G>A
ENST00000620295.2:c.4116G>A ENSP00000478500.1:p.Ser1372=
ENST00000622724.3:c.4080G>A ENSP00000480063.1:p.Ser1360=
ENST00000635499.1:c.203G>A
NM_015074.3:c.4020G>A , LRG_252t1:c.4020G>A NP_055889.2:p.Ser1340=
XR_946953.1:n.401+390C>T
NM_001365951.1:c.4158G>A NP_001352880.1:p.Ser1386=
NM_001365952.1:c.4158G>A NP_001352881.1:p.Ser1386=
XR_946953.2:n.276+390C>T
NM_001365951.3:c.4158G>A MANE Select NP_001352880.1:p.Ser1386=