Canonical Allele Identifier: CA1153153597

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10320007C= , CM000663.2:g.10320007C=	GRCh38
NC_000001.10:g.10380065C= , CM000663.1:g.10380065C=	GRCh37
NC_000001.9:g.10302652C=	NCBI36
NG_008069.1:g.114302C= , LRG_252:g.114302C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.1978-36C=	ENSP00000512668.1:n.1978-36C=
ENST00000696503.1:c.2041-36C=	ENSP00000512669.1:n.2041-36C=
ENST00000696504.1:c.2041-36C=	ENSP00000512670.1:n.2041-36C=
ENST00000676179.1:c.2116-36C= MANE Select	ENSP00000502065.1:n.2116-36C=
ENST00000263934.10:c.1978-36C=	ENSP00000263934.6:n.1978-36C=
ENST00000377081.5:c.2116-36C=	ENSP00000366284.1:n.2116-36C=
ENST00000377086.5:c.2116-36C=	ENSP00000366290.1:n.2116-36C=
ENST00000620295.2:c.2074-36C=	ENSP00000478500.1:n.2074-36C=
ENST00000622724.3:c.2038-36C=	ENSP00000480063.1:n.2038-36C=
NM_015074.3:c.1978-36C= , LRG_252t1:c.1978-36C=	NP_055889.2:n.1978-36C=
NM_001365951.1:c.2116-36C=	NP_001352880.1:n.2116-36C=
NM_001365952.1:c.2116-36C=	NP_001352881.1:n.2116-36C=
NM_001365951.3:c.2116-36C= MANE Select	NP_001352880.1:n.2116-36C=