Canonical Allele Identifier: CA338330786

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10435029C>A (hg19) ; chr1:g.10374971C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10374971C>A , CM000663.2:g.10374971C>A	GRCh38
NC_000001.10:g.10435029C>A , CM000663.1:g.10435029C>A	GRCh37
NC_000001.9:g.10357616C>A	NCBI36
NG_008069.1:g.169266C>A , LRG_252:g.169266C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.5277C>A	ENSP00000512668.1:p.Asp1759Glu
ENST00000696503.1:c.5139C>A	ENSP00000512669.1:p.Asp1713Glu
ENST00000696504.1:c.5139C>A	ENSP00000512670.1:p.Asp1713Glu
ENST00000676179.1:c.5214C>A MANE Select	ENSP00000502065.1:p.Asp1738Glu
ENST00000263934.10:c.5076C>A	ENSP00000263934.6:p.Asp1692Glu
ENST00000377081.5:c.5214C>A	ENSP00000366284.1:p.Asp1738Glu
ENST00000377086.5:c.5214C>A	ENSP00000366290.1:p.Asp1738Glu
ENST00000620295.2:c.5172C>A	ENSP00000478500.1:p.Asp1724Glu
ENST00000622724.3:c.5136C>A	ENSP00000480063.1:p.Asp1712Glu
ENST00000635499.1:c.1259C>A
NM_015074.3:c.5076C>A , LRG_252t1:c.5076C>A	NP_055889.2:p.Asp1692Glu
NM_001365951.1:c.5214C>A	NP_001352880.1:p.Asp1738Glu
NM_001365952.1:c.5214C>A	NP_001352881.1:p.Asp1738Glu
NM_001365951.3:c.5214C>A MANE Select	NP_001352880.1:p.Asp1738Glu