Canonical Allele Identifier: CA2643182302

Gene: KIF1B

Linked Data

• gnomAD v4: 1-10339632-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10339632C>A , CM000663.2:g.10339632C>A	GRCh38
NC_000001.10:g.10399690C>A , CM000663.1:g.10399690C>A	GRCh37
NC_000001.9:g.10322277C>A	NCBI36
NG_008069.1:g.133927C>A , LRG_252:g.133927C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3285-137C>A	ENSP00000512668.1:n.3285-137C>A
ENST00000696503.1:c.3348-137C>A	ENSP00000512669.1:n.3348-137C>A
ENST00000696504.1:c.3348-137C>A	ENSP00000512670.1:n.3348-137C>A
ENST00000676179.1:c.3423-137C>A MANE Select	ENSP00000502065.1:n.3423-137C>A
ENST00000263934.10:c.3285-137C>A	ENSP00000263934.6:n.3285-137C>A
ENST00000377081.5:c.3423-137C>A	ENSP00000366284.1:n.3423-137C>A
ENST00000377086.5:c.3423-137C>A	ENSP00000366290.1:n.3423-137C>A
ENST00000620295.2:c.3381-137C>A	ENSP00000478500.1:n.3381-137C>A
ENST00000622724.3:c.3345-137C>A	ENSP00000480063.1:n.3345-137C>A
NM_015074.3:c.3285-137C>A , LRG_252t1:c.3285-137C>A	NP_055889.2:n.3285-137C>A
NM_001365951.1:c.3423-137C>A	NP_001352880.1:n.3423-137C>A
NM_001365952.1:c.3423-137C>A	NP_001352881.1:n.3423-137C>A
NM_001365951.3:c.3423-137C>A MANE Select	NP_001352880.1:n.3423-137C>A