Canonical Allele Identifier: CA17836586
Gene: KIF1B HGNC NCBI

Linked Data

dbSNP Id: rs535523799

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10325362dup , CM000663.2:g.10325362dup GRCh38
NC_000001.10:g.10385420dup , CM000663.1:g.10385420dup GRCh37
NC_000001.9:g.10308007dup NCBI36
NG_008069.1:g.119657dup , LRG_252:g.119657dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696502.1:c.2537+467dup ENSP00000512668.1:n.2537+467dup
ENST00000696503.1:c.2600+467dup ENSP00000512669.1:n.2600+467dup
ENST00000696504.1:c.2600+467dup ENSP00000512670.1:n.2600+467dup
ENST00000676179.1:c.2675+467dup MANE Select ENSP00000502065.1:n.2675+467dup
ENST00000263934.10:c.2537+467dup ENSP00000263934.6:n.2537+467dup
ENST00000377081.5:c.2675+467dup ENSP00000366284.1:n.2675+467dup
ENST00000377086.5:c.2675+467dup ENSP00000366290.1:n.2675+467dup
ENST00000620295.2:c.2633+467dup ENSP00000478500.1:n.2633+467dup
ENST00000622724.3:c.2597+467dup ENSP00000480063.1:n.2597+467dup
NM_015074.3:c.2537+467dup , LRG_252t1:c.2537+467dup NP_055889.2:n.2537+467dup
NM_001365951.1:c.2675+467dup NP_001352880.1:n.2675+467dup
NM_001365952.1:c.2675+467dup NP_001352881.1:n.2675+467dup
NM_001365951.3:c.2675+467dup MANE Select NP_001352880.1:n.2675+467dup