Canonical Allele Identifier: CA521151172

Gene: KIF1B

Linked Data

• dbSNP Id: rs1421743455
• gnomAD v2: 1-10403349-AG-A
• gnomAD v4: 1-10343291-AG-A
• MyVariant Identifiers: chr1:g.10403350del (hg19) ; chr1:g.10343292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10343292del , CM000663.2:g.10343292del	GRCh38
NC_000001.10:g.10403350del , CM000663.1:g.10403350del	GRCh37
NC_000001.9:g.10325937del	NCBI36
NG_008069.1:g.137587del , LRG_252:g.137587del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3550+5del	ENSP00000512668.1:n.3550+5del
ENST00000696503.1:c.3613+5del	ENSP00000512669.1:n.3613+5del
ENST00000696504.1:c.3613+5del	ENSP00000512670.1:n.3613+5del
ENST00000676179.1:c.3688+5del MANE Select	ENSP00000502065.1:n.3688+5del
ENST00000263934.10:c.3550+5del	ENSP00000263934.6:n.3550+5del
ENST00000377081.5:c.3688+5del	ENSP00000366284.1:n.3688+5del
ENST00000377086.5:c.3688+5del	ENSP00000366290.1:n.3688+5del
ENST00000620295.2:c.3646+5del	ENSP00000478500.1:n.3646+5del
ENST00000622724.3:c.3610+5del	ENSP00000480063.1:n.3610+5del
NM_015074.3:c.3550+5del , LRG_252t1:c.3550+5del	NP_055889.2:n.3550+5del
NM_001365951.1:c.3688+5del	NP_001352880.1:n.3688+5del
NM_001365952.1:c.3688+5del	NP_001352881.1:n.3688+5del
NM_001365951.3:c.3688+5del MANE Select	NP_001352880.1:n.3688+5del