Canonical Allele Identifier: CA1153220754

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10378507_10378509delinsCCT , CM000663.2:g.10378507_10378509delinsCCT	GRCh38
NC_000001.10:g.10438565_10438567delinsCCT , CM000663.1:g.10438565_10438567delinsCCT	GRCh37
NC_000001.9:g.10361152_10361154delinsCCT	NCBI36
NG_008069.1:g.172802_172804delinsCCT , LRG_252:g.172802_172804delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676179.1:c.*1920_*1922delinsCCT MANE Select	ENSP00000502065.1:n.*1920_*1922delinsCCT
ENST00000377081.5:c.*105_*107delinsCCT	ENSP00000366284.1:n.*105_*107delinsCCT
ENST00000377086.5:c.*1920_*1922delinsCCT	ENSP00000366290.1:n.*1920_*1922delinsCCT
ENST00000620295.2:c.5535_5537delinsCCT	ENSP00000478500.1:n.5535_5537delinsCCT
ENST00000622724.3:c.5499_5501delinsCCT	ENSP00000480063.1:n.5499_5501delinsCCT
NM_015074.3:c.*1920_*1922delinsCCT , LRG_252t1:c.*1920_*1922delinsCCT	NP_055889.2:n.*1920_*1922delinsCCT
NM_001365951.1:c.*1920_*1922delinsCCT	NP_001352880.1:n.*1920_*1922delinsCCT
NM_001365952.1:c.*1920_*1922delinsCCT	NP_001352881.1:n.*1920_*1922delinsCCT
NM_001365951.3:c.*1920_*1922delinsCCT MANE Select	NP_001352880.1:n.*1920_*1922delinsCCT