Canonical Allele Identifier: CA2574206510
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10348573T>C , CM000663.2:g.10348573T>C GRCh38
NC_000001.10:g.10408631T>C , CM000663.1:g.10408631T>C GRCh37
NC_000001.9:g.10331218T>C NCBI36
NG_008069.1:g.142868T>C , LRG_252:g.142868T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696502.1:c.3928-76T>C ENSP00000512668.1:n.3928-76T>C
ENST00000696503.1:c.3790-76T>C ENSP00000512669.1:n.3790-76T>C
ENST00000696504.1:c.3790-76T>C ENSP00000512670.1:n.3790-76T>C
ENST00000676179.1:c.3865-76T>C MANE Select ENSP00000502065.1:n.3865-76T>C
ENST00000263934.10:c.3727-76T>C ENSP00000263934.6:n.3727-76T>C
ENST00000377081.5:c.3865-76T>C ENSP00000366284.1:n.3865-76T>C
ENST00000377086.5:c.3865-76T>C ENSP00000366290.1:n.3865-76T>C
ENST00000465635.5:n.320-76T>C
ENST00000483340.1:n.401-76T>C
ENST00000620295.2:c.3823-76T>C ENSP00000478500.1:n.3823-76T>C
ENST00000622724.3:c.3787-76T>C ENSP00000480063.1:n.3787-76T>C
NM_015074.3:c.3727-76T>C , LRG_252t1:c.3727-76T>C NP_055889.2:n.3727-76T>C
NM_001365951.1:c.3865-76T>C NP_001352880.1:n.3865-76T>C
NM_001365952.1:c.3865-76T>C NP_001352881.1:n.3865-76T>C
NM_001365951.3:c.3865-76T>C MANE Select NP_001352880.1:n.3865-76T>C