Canonical Allele Identifier: CA338342148
Gene: KIF1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10343276T>A , CM000663.2:g.10343276T>A GRCh38
NC_000001.10:g.10403334T>A , CM000663.1:g.10403334T>A GRCh37
NC_000001.9:g.10325921T>A NCBI36
NG_008069.1:g.137571T>A , LRG_252:g.137571T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3539T>A ENSP00000512668.1:p.Leu1180Gln
ENST00000696503.1:c.3602T>A ENSP00000512669.1:p.Leu1201Gln
ENST00000696504.1:c.3602T>A ENSP00000512670.1:p.Leu1201Gln
ENST00000676179.1:c.3677T>A MANE Select ENSP00000502065.1:p.Leu1226Gln
ENST00000263934.10:c.3539T>A ENSP00000263934.6:p.Leu1180Gln
ENST00000377081.5:c.3677T>A ENSP00000366284.1:p.Leu1226Gln
ENST00000377086.5:c.3677T>A ENSP00000366290.1:p.Leu1226Gln
ENST00000620295.2:c.3635T>A ENSP00000478500.1:p.Leu1212Gln
ENST00000622724.3:c.3599T>A ENSP00000480063.1:p.Leu1200Gln
NM_015074.3:c.3539T>A , LRG_252t1:c.3539T>A NP_055889.2:p.Leu1180Gln
NM_001365951.1:c.3677T>A NP_001352880.1:p.Leu1226Gln
NM_001365952.1:c.3677T>A NP_001352881.1:p.Leu1226Gln
NM_001365951.3:c.3677T>A MANE Select NP_001352880.1:p.Leu1226Gln