Canonical Allele Identifier: CA1153146201
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10345897G= , CM000663.2:g.10345897G= GRCh38
NC_000001.10:g.10405955G= , CM000663.1:g.10405955G= GRCh37
NC_000001.9:g.10328542G= NCBI36
NG_008069.1:g.140192G= , LRG_252:g.140192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3804G= ENSP00000512668.1:p.Met1268=
ENST00000696503.1:c.3666G= ENSP00000512669.1:p.Met1222=
ENST00000696504.1:c.3666G= ENSP00000512670.1:p.Met1222=
ENST00000676179.1:c.3741G= MANE Select ENSP00000502065.1:p.Met1247=
ENST00000263934.10:c.3603G= ENSP00000263934.6:p.Met1201=
ENST00000377081.5:c.3741G= ENSP00000366284.1:p.Met1247=
ENST00000377086.5:c.3741G= ENSP00000366290.1:p.Met1247=
ENST00000465635.5:n.196G=
ENST00000483340.1:n.277G=
ENST00000620295.2:c.3699G= ENSP00000478500.1:p.Met1233=
ENST00000622724.3:c.3663G= ENSP00000480063.1:p.Met1221=
NM_015074.3:c.3603G= , LRG_252t1:c.3603G= NP_055889.2:p.Met1201=
NM_001365951.1:c.3741G= NP_001352880.1:p.Met1247=
NM_001365952.1:c.3741G= NP_001352881.1:p.Met1247=
NM_001365951.3:c.3741G= MANE Select NP_001352880.1:p.Met1247=