Canonical Allele Identifier: CA338335849

Gene: KIF1B

Linked Data

• ClinVar Variation Id: 1792743
• ClinVar RCV Id: RCV004062135
• dbSNP Id: rs1379489043
• MyVariant Identifiers: chr1:g.10384950G>C (hg19) ; chr1:g.10324892G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324892G>C , CM000663.2:g.10324892G>C	GRCh38
NC_000001.10:g.10384950G>C , CM000663.1:g.10384950G>C	GRCh37
NC_000001.9:g.10307537G>C	NCBI36
NG_008069.1:g.119187G>C , LRG_252:g.119187G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.2534G>C	ENSP00000512668.1:p.Gly845Ala
ENST00000696503.1:c.2597G>C	ENSP00000512669.1:p.Gly866Ala
ENST00000696504.1:c.2597G>C	ENSP00000512670.1:p.Gly866Ala
ENST00000676179.1:c.2672G>C MANE Select	ENSP00000502065.1:p.Gly891Ala
ENST00000263934.10:c.2534G>C	ENSP00000263934.6:p.Gly845Ala
ENST00000377081.5:c.2672G>C	ENSP00000366284.1:p.Gly891Ala
ENST00000377086.5:c.2672G>C	ENSP00000366290.1:p.Gly891Ala
ENST00000620295.2:c.2630G>C	ENSP00000478500.1:p.Gly877Ala
ENST00000622724.3:c.2594G>C	ENSP00000480063.1:p.Gly865Ala
NM_015074.3:c.2534G>C , LRG_252t1:c.2534G>C	NP_055889.2:p.Gly845Ala
NM_001365951.1:c.2672G>C	NP_001352880.1:p.Gly891Ala
NM_001365952.1:c.2672G>C	NP_001352881.1:p.Gly891Ala
NM_001365951.3:c.2672G>C MANE Select	NP_001352880.1:p.Gly891Ala