Canonical Allele Identifier: CA415881676

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10384894C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324836C>A , CM000663.2:g.10324836C>A	GRCh38
NC_000001.10:g.10384894C>A , CM000663.1:g.10384894C>A	GRCh37
NC_000001.9:g.10307481C>A	NCBI36
NG_008069.1:g.119131C>A , LRG_252:g.119131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.2478C>A	ENSP00000512668.1:p.Thr826=
ENST00000696503.1:c.2541C>A	ENSP00000512669.1:p.Thr847=
ENST00000696504.1:c.2541C>A	ENSP00000512670.1:p.Thr847=
ENST00000676179.1:c.2616C>A MANE Select	ENSP00000502065.1:p.Thr872=
ENST00000263934.10:c.2478C>A	ENSP00000263934.6:p.Thr826=
ENST00000377081.5:c.2616C>A	ENSP00000366284.1:p.Thr872=
ENST00000377086.5:c.2616C>A	ENSP00000366290.1:p.Thr872=
ENST00000620295.2:c.2574C>A	ENSP00000478500.1:p.Thr858=
ENST00000622724.3:c.2538C>A	ENSP00000480063.1:p.Thr846=
NM_015074.3:c.2478C>A , LRG_252t1:c.2478C>A	NP_055889.2:p.Thr826=
NM_001365951.1:c.2616C>A	NP_001352880.1:p.Thr872=
NM_001365952.1:c.2616C>A	NP_001352881.1:p.Thr872=
NM_001365951.3:c.2616C>A MANE Select	NP_001352880.1:p.Thr872=