Canonical Allele Identifier: CA338323975

Gene: KIF1B

Linked Data

• gnomAD v4: 1-10368468-G-A
• MyVariant Identifiers: chr1:g.10428526G>A (hg19) ; chr1:g.10368468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368468G>A , CM000663.2:g.10368468G>A	GRCh38
NC_000001.10:g.10428526G>A , CM000663.1:g.10428526G>A	GRCh37
NC_000001.9:g.10351113G>A	NCBI36
NG_008069.1:g.162763G>A , LRG_252:g.162763G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4817G>A	ENSP00000512668.1:p.Cys1606Tyr
ENST00000696503.1:c.4679G>A	ENSP00000512669.1:p.Cys1560Tyr
ENST00000696504.1:c.4679G>A	ENSP00000512670.1:p.Cys1560Tyr
ENST00000676179.1:c.4754G>A MANE Select	ENSP00000502065.1:p.Cys1585Tyr
ENST00000263934.10:c.4616G>A	ENSP00000263934.6:p.Cys1539Tyr
ENST00000377081.5:c.4754G>A	ENSP00000366284.1:p.Cys1585Tyr
ENST00000377086.5:c.4754G>A	ENSP00000366290.1:p.Cys1585Tyr
ENST00000470616.1:n.485G>A
ENST00000620295.2:c.4712G>A	ENSP00000478500.1:p.Cys1571Tyr
ENST00000622724.3:c.4676G>A	ENSP00000480063.1:p.Cys1559Tyr
ENST00000635499.1:c.799G>A
NM_015074.3:c.4616G>A , LRG_252t1:c.4616G>A	NP_055889.2:p.Cys1539Tyr
NM_001365951.1:c.4754G>A	NP_001352880.1:p.Cys1585Tyr
NM_001365952.1:c.4754G>A	NP_001352881.1:p.Cys1585Tyr
NM_001365951.3:c.4754G>A MANE Select	NP_001352880.1:p.Cys1585Tyr