Canonical Allele Identifier: CA1153147272
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10348672G= , CM000663.2:g.10348672G= GRCh38
NC_000001.10:g.10408730G= , CM000663.1:g.10408730G= GRCh37
NC_000001.9:g.10331317G= NCBI36
NG_008069.1:g.142967G= , LRG_252:g.142967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3951G= ENSP00000512668.1:p.Val1317=
ENST00000696503.1:c.3813G= ENSP00000512669.1:p.Val1271=
ENST00000696504.1:c.3813G= ENSP00000512670.1:p.Val1271=
ENST00000676179.1:c.3888G= MANE Select ENSP00000502065.1:p.Val1296=
ENST00000263934.10:c.3750G= ENSP00000263934.6:p.Val1250=
ENST00000377081.5:c.3888G= ENSP00000366284.1:p.Val1296=
ENST00000377086.5:c.3888G= ENSP00000366290.1:p.Val1296=
ENST00000465635.5:n.343G=
ENST00000483340.1:n.424G=
ENST00000620295.2:c.3846G= ENSP00000478500.1:p.Val1282=
ENST00000622724.3:c.3810G= ENSP00000480063.1:p.Val1270=
NM_015074.3:c.3750G= , LRG_252t1:c.3750G= NP_055889.2:p.Val1250=
NM_001365951.1:c.3888G= NP_001352880.1:p.Val1296=
NM_001365952.1:c.3888G= NP_001352881.1:p.Val1296=
NM_001365951.3:c.3888G= MANE Select NP_001352880.1:p.Val1296=