Canonical Allele Identifier: CA415881403

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10380146C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10320088C>A , CM000663.2:g.10320088C>A	GRCh38
NC_000001.10:g.10380146C>A , CM000663.1:g.10380146C>A	GRCh37
NC_000001.9:g.10302733C>A	NCBI36
NG_008069.1:g.114383C>A , LRG_252:g.114383C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.2023C>A	ENSP00000512668.1:p.Arg675=
ENST00000696503.1:c.2086C>A	ENSP00000512669.1:p.Arg696=
ENST00000696504.1:c.2086C>A	ENSP00000512670.1:p.Arg696=
ENST00000676179.1:c.2161C>A MANE Select	ENSP00000502065.1:p.Arg721=
ENST00000263934.10:c.2023C>A	ENSP00000263934.6:p.Arg675=
ENST00000377081.5:c.2161C>A	ENSP00000366284.1:p.Arg721=
ENST00000377086.5:c.2161C>A	ENSP00000366290.1:p.Arg721=
ENST00000620295.2:c.2119C>A	ENSP00000478500.1:p.Arg707=
ENST00000622724.3:c.2083C>A	ENSP00000480063.1:p.Arg695=
NM_015074.3:c.2023C>A , LRG_252t1:c.2023C>A	NP_055889.2:p.Arg675=
NM_001365951.1:c.2161C>A	NP_001352880.1:p.Arg721=
NM_001365952.1:c.2161C>A	NP_001352881.1:p.Arg721=
NM_001365951.3:c.2161C>A MANE Select	NP_001352880.1:p.Arg721=