Canonical Allele Identifier: CA582111

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365418A>G , CM000663.2:g.10365418A>G	GRCh38
NC_000001.10:g.10425476A>G , CM000663.1:g.10425476A>G	GRCh37
NC_000001.9:g.10348063A>G	NCBI36
NG_008069.1:g.159713A>G , LRG_252:g.159713A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4522A>G MANE Select	NP_001352880.1:p.Thr1508Ala
ENST00000676179.1:c.4522A>G MANE Select	ENSP00000502065.1:p.Thr1508Ala
NM_001365951.1:c.4522A>G	NP_001352880.1:p.Thr1508Ala
NM_001365952.1:c.4522A>G	NP_001352881.1:p.Thr1508Ala
NM_015074.3:c.4384A>G , LRG_252t1:c.4384A>G	NP_055889.2:p.Thr1462Ala
ENST00000263934.10:c.4384A>G	ENSP00000263934.6:p.Thr1462Ala
ENST00000377081.5:c.4522A>G	ENSP00000366284.1:p.Thr1508Ala
ENST00000377086.5:c.4522A>G	ENSP00000366290.1:p.Thr1508Ala
ENST00000470616.1:n.253A>G
ENST00000620295.2:c.4480A>G	ENSP00000478500.1:p.Thr1494Ala
ENST00000622724.3:c.4444A>G	ENSP00000480063.1:p.Thr1482Ala
ENST00000635499.1:c.567A>G
ENST00000696502.1:c.4585A>G	ENSP00000512668.1:p.Thr1529Ala
ENST00000696503.1:c.4447A>G	ENSP00000512669.1:p.Thr1483Ala
ENST00000696504.1:c.4447A>G	ENSP00000512670.1:p.Thr1483Ala
XR_946953.1:n.355+963T>C
XR_946953.2:n.230+963T>C