Canonical Allele Identifier: CA338342402

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10405950A>T (hg19) ; chr1:g.10345892A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345892A>T , CM000663.2:g.10345892A>T	GRCh38
NC_000001.10:g.10405950A>T , CM000663.1:g.10405950A>T	GRCh37
NC_000001.9:g.10328537A>T	NCBI36
NG_008069.1:g.140187A>T , LRG_252:g.140187A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3799A>T	ENSP00000512668.1:p.Ser1267Cys
ENST00000696503.1:c.3661A>T	ENSP00000512669.1:p.Ser1221Cys
ENST00000696504.1:c.3661A>T	ENSP00000512670.1:p.Ser1221Cys
ENST00000676179.1:c.3736A>T MANE Select	ENSP00000502065.1:p.Ser1246Cys
ENST00000263934.10:c.3598A>T	ENSP00000263934.6:p.Ser1200Cys
ENST00000377081.5:c.3736A>T	ENSP00000366284.1:p.Ser1246Cys
ENST00000377086.5:c.3736A>T	ENSP00000366290.1:p.Ser1246Cys
ENST00000465635.5:n.191A>T
ENST00000483340.1:n.272A>T
ENST00000620295.2:c.3694A>T	ENSP00000478500.1:p.Ser1232Cys
ENST00000622724.3:c.3658A>T	ENSP00000480063.1:p.Ser1220Cys
NM_015074.3:c.3598A>T , LRG_252t1:c.3598A>T	NP_055889.2:p.Ser1200Cys
NM_001365951.1:c.3736A>T	NP_001352880.1:p.Ser1246Cys
NM_001365952.1:c.3736A>T	NP_001352881.1:p.Ser1246Cys
NM_001365951.3:c.3736A>T MANE Select	NP_001352880.1:p.Ser1246Cys