Canonical Allele Identifier: CA582207
Community Standard Title: NM_001365951.3(KIF1B):c.4843A>G (p.Ile1615Val)
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10371159A>G , CM000663.2:g.10371159A>G GRCh38
NC_000001.10:g.10431217A>G , CM000663.1:g.10431217A>G GRCh37
NC_000001.9:g.10353804A>G NCBI36
NG_008069.1:g.165454A>G , LRG_252:g.165454A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001365951.3:c.4843A>G MANE Select NP_001352880.1:p.Ile1615Val
ENST00000676179.1:c.4843A>G MANE Select ENSP00000502065.1:p.Ile1615Val
NM_001365951.1:c.4843A>G NP_001352880.1:p.Ile1615Val
NM_001365952.1:c.4843A>G NP_001352881.1:p.Ile1615Val
NM_015074.3:c.4705A>G , LRG_252t1:c.4705A>G NP_055889.2:p.Ile1569Val
ENST00000263934.10:c.4705A>G ENSP00000263934.6:p.Ile1569Val
ENST00000377081.5:c.4843A>G ENSP00000366284.1:p.Ile1615Val
ENST00000377086.5:c.4843A>G ENSP00000366290.1:p.Ile1615Val
ENST00000620295.2:c.4801A>G ENSP00000478500.1:p.Ile1601Val
ENST00000622724.3:c.4765A>G ENSP00000480063.1:p.Ile1589Val
ENST00000635499.1:c.888A>G
ENST00000696502.1:c.4906A>G ENSP00000512668.1:p.Ile1636Val
ENST00000696503.1:c.4768A>G ENSP00000512669.1:p.Ile1590Val
ENST00000696504.1:c.4768A>G ENSP00000512670.1:p.Ile1590Val