Canonical Allele Identifier: CA998520162

Gene: KIF1B

Linked Data

• dbSNP Id: rs1638950326
• gnomAD v3: 1-10378682-T-TTG
• gnomAD v4: 1-10378682-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10378686_10378687dup , CM000663.2:g.10378686_10378687dup	GRCh38
NC_000001.10:g.10438744_10438745dup , CM000663.1:g.10438744_10438745dup	GRCh37
NC_000001.9:g.10361331_10361332dup	NCBI36
NG_008069.1:g.172981_172982dup , LRG_252:g.172981_172982dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000676179.1:c.*2099_*2100dup MANE Select	ENSP00000502065.1:n.*2099_*2100dup
ENST00000377081.5:c.*284_*285dup	ENSP00000366284.1:n.*284_*285dup
ENST00000377086.5:c.*2099_*2100dup	ENSP00000366290.1:n.*2099_*2100dup
ENST00000620295.2:c.5714_5715dup	ENSP00000478500.1:n.5714_5715dup
ENST00000622724.3:c.5678_5679dup	ENSP00000480063.1:n.5678_5679dup
NM_015074.3:c.*2099_*2100dup , LRG_252t1:c.*2099_*2100dup	NP_055889.2:n.*2099_*2100dup
NM_001365951.1:c.*2099_*2100dup	NP_001352880.1:n.*2099_*2100dup
NM_001365952.1:c.*2099_*2100dup	NP_001352881.1:n.*2099_*2100dup
NM_001365951.3:c.*2099_*2100dup MANE Select	NP_001352880.1:n.*2099_*2100dup