Canonical Allele Identifier: CA17856405
Community Standard Title: NM_001365951.3(KIF1B):c.5231T>C (p.Ile1744Thr)
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10374988T>C , CM000663.2:g.10374988T>C GRCh38
NC_000001.10:g.10435046T>C , CM000663.1:g.10435046T>C GRCh37
NC_000001.9:g.10357633T>C NCBI36
NG_008069.1:g.169283T>C , LRG_252:g.169283T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001365951.3:c.5231T>C MANE Select NP_001352880.1:p.Ile1744Thr
ENST00000676179.1:c.5231T>C MANE Select ENSP00000502065.1:p.Ile1744Thr
NM_001365951.1:c.5231T>C NP_001352880.1:p.Ile1744Thr
NM_001365952.1:c.5231T>C NP_001352881.1:p.Ile1744Thr
NM_015074.3:c.5093T>C , LRG_252t1:c.5093T>C NP_055889.2:p.Ile1698Thr
ENST00000263934.10:c.5093T>C ENSP00000263934.6:p.Ile1698Thr
ENST00000377081.5:c.5231T>C ENSP00000366284.1:p.Ile1744Thr
ENST00000377086.5:c.5231T>C ENSP00000366290.1:p.Ile1744Thr
ENST00000620295.2:c.5189T>C ENSP00000478500.1:p.Ile1730Thr
ENST00000622724.3:c.5153T>C ENSP00000480063.1:p.Ile1718Thr
ENST00000635499.1:c.1276T>C
ENST00000696502.1:c.5294T>C ENSP00000512668.1:p.Ile1765Thr
ENST00000696503.1:c.5156T>C ENSP00000512669.1:p.Ile1719Thr
ENST00000696504.1:c.5156T>C ENSP00000512670.1:p.Ile1719Thr