Canonical Allele Identifier: CA338340417

Gene: KIF1B

Linked Data

• dbSNP Id: rs1569853886
• MyVariant Identifiers: chr1:g.10397476T>G (hg19) ; chr1:g.10337418T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10337418T>G , CM000663.2:g.10337418T>G	GRCh38
NC_000001.10:g.10397476T>G , CM000663.1:g.10397476T>G	GRCh37
NC_000001.9:g.10320063T>G	NCBI36
NG_008069.1:g.131713T>G , LRG_252:g.131713T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.3169T>G	ENSP00000512668.1:p.Phe1057Val
ENST00000696503.1:c.3232T>G	ENSP00000512669.1:p.Phe1078Val
ENST00000696504.1:c.3232T>G	ENSP00000512670.1:p.Phe1078Val
ENST00000676179.1:c.3307T>G MANE Select	ENSP00000502065.1:p.Phe1103Val
ENST00000263934.10:c.3169T>G	ENSP00000263934.6:p.Phe1057Val
ENST00000377081.5:c.3307T>G	ENSP00000366284.1:p.Phe1103Val
ENST00000377086.5:c.3307T>G	ENSP00000366290.1:p.Phe1103Val
ENST00000620295.2:c.3265T>G	ENSP00000478500.1:p.Phe1089Val
ENST00000622724.3:c.3229T>G	ENSP00000480063.1:p.Phe1077Val
NM_015074.3:c.3169T>G , LRG_252t1:c.3169T>G	NP_055889.2:p.Phe1057Val
NM_001365951.1:c.3307T>G	NP_001352880.1:p.Phe1103Val
NM_001365952.1:c.3307T>G	NP_001352881.1:p.Phe1103Val
NM_001365951.3:c.3307T>G MANE Select	NP_001352880.1:p.Phe1103Val