Canonical Allele Identifier: CA1153147274

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348675C= , CM000663.2:g.10348675C=	GRCh38
NC_000001.10:g.10408733C= , CM000663.1:g.10408733C=	GRCh37
NC_000001.9:g.10331320C=	NCBI36
NG_008069.1:g.142970C= , LRG_252:g.142970C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.3954C=	ENSP00000512668.1:p.Thr1318=
ENST00000696503.1:c.3816C=	ENSP00000512669.1:p.Thr1272=
ENST00000696504.1:c.3816C=	ENSP00000512670.1:p.Thr1272=
ENST00000676179.1:c.3891C= MANE Select	ENSP00000502065.1:p.Thr1297=
ENST00000263934.10:c.3753C=	ENSP00000263934.6:p.Thr1251=
ENST00000377081.5:c.3891C=	ENSP00000366284.1:p.Thr1297=
ENST00000377086.5:c.3891C=	ENSP00000366290.1:p.Thr1297=
ENST00000465635.5:n.346C=
ENST00000483340.1:n.427C=
ENST00000620295.2:c.3849C=	ENSP00000478500.1:p.Thr1283=
ENST00000622724.3:c.3813C=	ENSP00000480063.1:p.Thr1271=
NM_015074.3:c.3753C= , LRG_252t1:c.3753C=	NP_055889.2:p.Thr1251=
NM_001365951.1:c.3891C=	NP_001352880.1:p.Thr1297=
NM_001365952.1:c.3891C=	NP_001352881.1:p.Thr1297=
NM_001365951.3:c.3891C= MANE Select	NP_001352880.1:p.Thr1297=