Canonical Allele Identifier: CA338321897

Gene: KIF1B

Linked Data

• ClinVar Variation Id: 1693791
• ClinVar RCV Id: RCV002261660
• dbSNP Id: rs2102350303
• MyVariant Identifiers: chr1:g.10425524A>G (hg19) ; chr1:g.10365466A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365466A>G , CM000663.2:g.10365466A>G	GRCh38
NC_000001.10:g.10425524A>G , CM000663.1:g.10425524A>G	GRCh37
NC_000001.9:g.10348111A>G	NCBI36
NG_008069.1:g.159761A>G , LRG_252:g.159761A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4633A>G	ENSP00000512668.1:p.Lys1545Glu
ENST00000696503.1:c.4495A>G	ENSP00000512669.1:p.Lys1499Glu
ENST00000696504.1:c.4495A>G	ENSP00000512670.1:p.Lys1499Glu
ENST00000676179.1:c.4570A>G MANE Select	ENSP00000502065.1:p.Lys1524Glu
ENST00000263934.10:c.4432A>G	ENSP00000263934.6:p.Lys1478Glu
ENST00000377081.5:c.4570A>G	ENSP00000366284.1:p.Lys1524Glu
ENST00000377086.5:c.4570A>G	ENSP00000366290.1:p.Lys1524Glu
ENST00000470616.1:n.301A>G
ENST00000620295.2:c.4528A>G	ENSP00000478500.1:p.Lys1510Glu
ENST00000622724.3:c.4492A>G	ENSP00000480063.1:p.Lys1498Glu
ENST00000635499.1:c.615A>G
NM_015074.3:c.4432A>G , LRG_252t1:c.4432A>G	NP_055889.2:p.Lys1478Glu
XR_946953.1:n.355+915T>C
NM_001365951.1:c.4570A>G	NP_001352880.1:p.Lys1524Glu
NM_001365952.1:c.4570A>G	NP_001352881.1:p.Lys1524Glu
XR_946953.2:n.230+915T>C
NM_001365951.3:c.4570A>G MANE Select	NP_001352880.1:p.Lys1524Glu