Canonical Allele Identifier: CA415888591

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10374929C>T , CM000663.2:g.10374929C>T	GRCh38
NC_000001.10:g.10434987C>T , CM000663.1:g.10434987C>T	GRCh37
NC_000001.9:g.10357574C>T	NCBI36
NG_008069.1:g.169224C>T , LRG_252:g.169224C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.5172C>T MANE Select	NP_001352880.1:p.Val1724=
ENST00000676179.1:c.5172C>T MANE Select	ENSP00000502065.1:p.Val1724=
NM_001365951.1:c.5172C>T	NP_001352880.1:p.Val1724=
NM_001365952.1:c.5172C>T	NP_001352881.1:p.Val1724=
NM_015074.3:c.5034C>T , LRG_252t1:c.5034C>T	NP_055889.2:p.Val1678=
ENST00000263934.10:c.5034C>T	ENSP00000263934.6:p.Val1678=
ENST00000377081.5:c.5172C>T	ENSP00000366284.1:p.Val1724=
ENST00000377086.5:c.5172C>T	ENSP00000366290.1:p.Val1724=
ENST00000620295.2:c.5130C>T	ENSP00000478500.1:p.Val1710=
ENST00000622724.3:c.5094C>T	ENSP00000480063.1:p.Val1698=
ENST00000635499.1:c.1217C>T
ENST00000696502.1:c.5235C>T	ENSP00000512668.1:p.Val1745=
ENST00000696503.1:c.5097C>T	ENSP00000512669.1:p.Val1699=
ENST00000696504.1:c.5097C>T	ENSP00000512670.1:p.Val1699=