Canonical Allele Identifier: CA1143425089

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10361732T= , CM000663.2:g.10361732T=	GRCh38
NC_000001.10:g.10421790T= , CM000663.1:g.10421790T=	GRCh37
NC_000001.9:g.10344377T=	NCBI36
NG_008069.1:g.156027T= , LRG_252:g.156027T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4211T= MANE Select	NP_001352880.1:p.Val1404=
ENST00000676179.1:c.4211T= MANE Select	ENSP00000502065.1:p.Val1404=
NM_001365951.1:c.4211T=	NP_001352880.1:p.Val1404=
NM_001365952.1:c.4211T=	NP_001352881.1:p.Val1404=
NM_015074.3:c.4073T= , LRG_252t1:c.4073T=	NP_055889.2:p.Val1358=
ENST00000263934.10:c.4073T=	ENSP00000263934.6:p.Val1358=
ENST00000377081.5:c.4211T=	ENSP00000366284.1:p.Val1404=
ENST00000377086.5:c.4211T=	ENSP00000366290.1:p.Val1404=
ENST00000465635.5:n.666T=
ENST00000483340.1:n.747T=
ENST00000620295.2:c.4169T=	ENSP00000478500.1:p.Val1390=
ENST00000622724.3:c.4133T=	ENSP00000480063.1:p.Val1378=
ENST00000635499.1:c.256T=
ENST00000696502.1:c.4274T=	ENSP00000512668.1:p.Val1425=
ENST00000696503.1:c.4136T=	ENSP00000512669.1:p.Val1379=
ENST00000696504.1:c.4136T=	ENSP00000512670.1:p.Val1379=
XR_946953.1:n.356-266A=
XR_946953.2:n.231-266A=