Canonical Allele Identifier: CA884819073

Gene: KIF1B

Linked Data

• dbSNP Id: rs1465286692
• MyVariant Identifiers: chr1:g.10428344del (hg19) ; chr1:g.10368286del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368287del , CM000663.2:g.10368287del	GRCh38
NC_000001.10:g.10428345del , CM000663.1:g.10428345del	GRCh37
NC_000001.9:g.10350932del	NCBI36
NG_008069.1:g.162582del , LRG_252:g.162582del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.4816-180del	ENSP00000512668.1:n.4816-180del
ENST00000696503.1:c.4678-180del	ENSP00000512669.1:n.4678-180del
ENST00000696504.1:c.4678-180del	ENSP00000512670.1:n.4678-180del
ENST00000676179.1:c.4753-180del MANE Select	ENSP00000502065.1:n.4753-180del
ENST00000263934.10:c.4615-180del	ENSP00000263934.6:n.4615-180del
ENST00000377081.5:c.4753-180del	ENSP00000366284.1:n.4753-180del
ENST00000377086.5:c.4753-180del	ENSP00000366290.1:n.4753-180del
ENST00000470616.1:n.484-180del
ENST00000620295.2:c.4711-180del	ENSP00000478500.1:n.4711-180del
ENST00000622724.3:c.4675-180del	ENSP00000480063.1:n.4675-180del
ENST00000635499.1:c.798-180del
NM_015074.3:c.4615-180del , LRG_252t1:c.4615-180del	NP_055889.2:n.4615-180del
NM_001365951.1:c.4753-180del	NP_001352880.1:n.4753-180del
NM_001365952.1:c.4753-180del	NP_001352881.1:n.4753-180del
NM_001365951.3:c.4753-180del MANE Select	NP_001352880.1:n.4753-180del