Canonical Allele Identifier: CA1141580572

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365476G= , CM000663.2:g.10365476G=	GRCh38
NC_000001.10:g.10425534G= , CM000663.1:g.10425534G=	GRCh37
NC_000001.9:g.10348121G=	NCBI36
NG_008069.1:g.159771G= , LRG_252:g.159771G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4580G= MANE Select	NP_001352880.1:p.Ser1527=
ENST00000676179.1:c.4580G= MANE Select	ENSP00000502065.1:p.Ser1527=
NM_001365951.1:c.4580G=	NP_001352880.1:p.Ser1527=
NM_001365952.1:c.4580G=	NP_001352881.1:p.Ser1527=
NM_015074.3:c.4442G= , LRG_252t1:c.4442G=	NP_055889.2:p.Ser1481=
ENST00000263934.10:c.4442G=	ENSP00000263934.6:p.Ser1481=
ENST00000377081.5:c.4580G=	ENSP00000366284.1:p.Ser1527=
ENST00000377086.5:c.4580G=	ENSP00000366290.1:p.Ser1527=
ENST00000470616.1:n.311G=
ENST00000620295.2:c.4538G=	ENSP00000478500.1:p.Ser1513=
ENST00000622724.3:c.4502G=	ENSP00000480063.1:p.Ser1501=
ENST00000635499.1:c.625G=
ENST00000696502.1:c.4643G=	ENSP00000512668.1:p.Ser1548=
ENST00000696503.1:c.4505G=	ENSP00000512669.1:p.Ser1502=
ENST00000696504.1:c.4505G=	ENSP00000512670.1:p.Ser1502=
XR_946953.1:n.355+905C=
XR_946953.2:n.230+905C=