Canonical Allele Identifier: CA415884349
Gene: KIF1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.10403338C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10343280C>A , CM000663.2:g.10343280C>A GRCh38
NC_000001.10:g.10403338C>A , CM000663.1:g.10403338C>A GRCh37
NC_000001.9:g.10325925C>A NCBI36
NG_008069.1:g.137575C>A , LRG_252:g.137575C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3543C>A ENSP00000512668.1:p.Ser1181=
ENST00000696503.1:c.3606C>A ENSP00000512669.1:p.Ser1202=
ENST00000696504.1:c.3606C>A ENSP00000512670.1:p.Ser1202=
ENST00000676179.1:c.3681C>A MANE Select ENSP00000502065.1:p.Ser1227=
ENST00000263934.10:c.3543C>A ENSP00000263934.6:p.Ser1181=
ENST00000377081.5:c.3681C>A ENSP00000366284.1:p.Ser1227=
ENST00000377086.5:c.3681C>A ENSP00000366290.1:p.Ser1227=
ENST00000620295.2:c.3639C>A ENSP00000478500.1:p.Ser1213=
ENST00000622724.3:c.3603C>A ENSP00000480063.1:p.Ser1201=
NM_015074.3:c.3543C>A , LRG_252t1:c.3543C>A NP_055889.2:p.Ser1181=
NM_001365951.1:c.3681C>A NP_001352880.1:p.Ser1227=
NM_001365952.1:c.3681C>A NP_001352881.1:p.Ser1227=
NM_001365951.3:c.3681C>A MANE Select NP_001352880.1:p.Ser1227=