Canonical Allele Identifier: CA582100

Gene: KIF1B

Linked Data

• dbSNP Id: rs369508428
• ExAC: 1:10425426 G / A
• gnomAD v2: 1-10425426-G-A
• gnomAD v3: 1-10365368-G-A
• gnomAD v4: 1-10365368-G-A
• MyVariant Identifiers: chr1:g.10425426G>A (hg19) ; chr1:g.10365368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365368G>A , CM000663.2:g.10365368G>A	GRCh38
NC_000001.10:g.10425426G>A , CM000663.1:g.10425426G>A	GRCh37
NC_000001.9:g.10348013G>A	NCBI36
NG_008069.1:g.159663G>A , LRG_252:g.159663G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.4576-41G>A	ENSP00000512668.1:n.4576-41G>A
ENST00000696503.1:c.4438-41G>A	ENSP00000512669.1:n.4438-41G>A
ENST00000696504.1:c.4438-41G>A	ENSP00000512670.1:n.4438-41G>A
ENST00000676179.1:c.4513-41G>A MANE Select	ENSP00000502065.1:n.4513-41G>A
ENST00000263934.10:c.4375-41G>A	ENSP00000263934.6:n.4375-41G>A
ENST00000377081.5:c.4513-41G>A	ENSP00000366284.1:n.4513-41G>A
ENST00000377086.5:c.4513-41G>A	ENSP00000366290.1:n.4513-41G>A
ENST00000470616.1:n.203G>A
ENST00000620295.2:c.4471-41G>A	ENSP00000478500.1:n.4471-41G>A
ENST00000622724.3:c.4435-41G>A	ENSP00000480063.1:n.4435-41G>A
ENST00000635499.1:c.558-41G>A
NM_015074.3:c.4375-41G>A , LRG_252t1:c.4375-41G>A	NP_055889.2:n.4375-41G>A
XR_946953.1:n.355+1013C>T
NM_001365951.1:c.4513-41G>A	NP_001352880.1:n.4513-41G>A
NM_001365952.1:c.4513-41G>A	NP_001352881.1:n.4513-41G>A
XR_946953.2:n.230+1013C>T
NM_001365951.3:c.4513-41G>A MANE Select	NP_001352880.1:n.4513-41G>A