Canonical Allele Identifier: CA582028

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10361818C>A , CM000663.2:g.10361818C>A	GRCh38
NC_000001.10:g.10421876C>A , CM000663.1:g.10421876C>A	GRCh37
NC_000001.9:g.10344463C>A	NCBI36
NG_008069.1:g.156113C>A , LRG_252:g.156113C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4297C>A MANE Select	NP_001352880.1:p.Pro1433Thr
ENST00000676179.1:c.4297C>A MANE Select	ENSP00000502065.1:p.Pro1433Thr
NM_001365951.1:c.4297C>A	NP_001352880.1:p.Pro1433Thr
NM_001365952.1:c.4297C>A	NP_001352881.1:p.Pro1433Thr
NM_015074.3:c.4159C>A , LRG_252t1:c.4159C>A	NP_055889.2:p.Pro1387Thr
ENST00000263934.10:c.4159C>A	ENSP00000263934.6:p.Pro1387Thr
ENST00000377081.5:c.4297C>A	ENSP00000366284.1:p.Pro1433Thr
ENST00000377086.5:c.4297C>A	ENSP00000366290.1:p.Pro1433Thr
ENST00000465635.5:n.752C>A
ENST00000483340.1:n.833C>A
ENST00000620295.2:c.4255C>A	ENSP00000478500.1:p.Pro1419Thr
ENST00000622724.3:c.4219C>A	ENSP00000480063.1:p.Pro1407Thr
ENST00000635499.1:c.342C>A
ENST00000696502.1:c.4360C>A	ENSP00000512668.1:p.Pro1454Thr
ENST00000696503.1:c.4222C>A	ENSP00000512669.1:p.Pro1408Thr
ENST00000696504.1:c.4222C>A	ENSP00000512670.1:p.Pro1408Thr
XR_946953.1:n.356-352G>T
XR_946953.2:n.231-352G>T