Canonical Allele Identifier: CA338321390

Gene: KIF1B

Linked Data

• gnomAD v4: 1-10365407-A-G
• MyVariant Identifiers: chr1:g.10425465A>G (hg19) ; chr1:g.10365407A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365407A>G , CM000663.2:g.10365407A>G	GRCh38
NC_000001.10:g.10425465A>G , CM000663.1:g.10425465A>G	GRCh37
NC_000001.9:g.10348052A>G	NCBI36
NG_008069.1:g.159702A>G , LRG_252:g.159702A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4576-2A>G	ENSP00000512668.1:n.4576-2A>G
ENST00000696503.1:c.4438-2A>G	ENSP00000512669.1:n.4438-2A>G
ENST00000696504.1:c.4438-2A>G	ENSP00000512670.1:n.4438-2A>G
ENST00000676179.1:c.4513-2A>G MANE Select	ENSP00000502065.1:n.4513-2A>G
ENST00000263934.10:c.4375-2A>G	ENSP00000263934.6:n.4375-2A>G
ENST00000377081.5:c.4513-2A>G	ENSP00000366284.1:n.4513-2A>G
ENST00000377086.5:c.4513-2A>G	ENSP00000366290.1:n.4513-2A>G
ENST00000470616.1:n.242A>G
ENST00000620295.2:c.4471-2A>G	ENSP00000478500.1:n.4471-2A>G
ENST00000622724.3:c.4435-2A>G	ENSP00000480063.1:n.4435-2A>G
ENST00000635499.1:c.558-2A>G
NM_015074.3:c.4375-2A>G , LRG_252t1:c.4375-2A>G	NP_055889.2:n.4375-2A>G
XR_946953.1:n.355+974T>C
NM_001365951.1:c.4513-2A>G	NP_001352880.1:n.4513-2A>G
NM_001365952.1:c.4513-2A>G	NP_001352881.1:n.4513-2A>G
XR_946953.2:n.230+974T>C
NM_001365951.3:c.4513-2A>G MANE Select	NP_001352880.1:n.4513-2A>G