Canonical Allele Identifier: CA1153146237
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10346012A= , CM000663.2:g.10346012A= GRCh38
NC_000001.10:g.10406070A= , CM000663.1:g.10406070A= GRCh37
NC_000001.9:g.10328657A= NCBI36
NG_008069.1:g.140307A= , LRG_252:g.140307A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3860+59A= ENSP00000512668.1:n.3860+59A=
ENST00000696503.1:c.3722+59A= ENSP00000512669.1:n.3722+59A=
ENST00000696504.1:c.3722+59A= ENSP00000512670.1:n.3722+59A=
ENST00000676179.1:c.3797+59A= MANE Select ENSP00000502065.1:n.3797+59A=
ENST00000263934.10:c.3659+59A= ENSP00000263934.6:n.3659+59A=
ENST00000377081.5:c.3797+59A= ENSP00000366284.1:n.3797+59A=
ENST00000377086.5:c.3797+59A= ENSP00000366290.1:n.3797+59A=
ENST00000465635.5:n.252+59A=
ENST00000483340.1:n.333+59A=
ENST00000620295.2:c.3755+59A= ENSP00000478500.1:n.3755+59A=
ENST00000622724.3:c.3719+59A= ENSP00000480063.1:n.3719+59A=
NM_015074.3:c.3659+59A= , LRG_252t1:c.3659+59A= NP_055889.2:n.3659+59A=
NM_001365951.1:c.3797+59A= NP_001352880.1:n.3797+59A=
NM_001365952.1:c.3797+59A= NP_001352881.1:n.3797+59A=
NM_001365951.3:c.3797+59A= MANE Select NP_001352880.1:n.3797+59A=