Canonical Allele Identifier: CA415884472

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10405988C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345930C>A , CM000663.2:g.10345930C>A	GRCh38
NC_000001.10:g.10405988C>A , CM000663.1:g.10405988C>A	GRCh37
NC_000001.9:g.10328575C>A	NCBI36
NG_008069.1:g.140225C>A , LRG_252:g.140225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3837C>A	ENSP00000512668.1:p.Ile1279=
ENST00000696503.1:c.3699C>A	ENSP00000512669.1:p.Ile1233=
ENST00000696504.1:c.3699C>A	ENSP00000512670.1:p.Ile1233=
ENST00000676179.1:c.3774C>A MANE Select	ENSP00000502065.1:p.Ile1258=
ENST00000263934.10:c.3636C>A	ENSP00000263934.6:p.Ile1212=
ENST00000377081.5:c.3774C>A	ENSP00000366284.1:p.Ile1258=
ENST00000377086.5:c.3774C>A	ENSP00000366290.1:p.Ile1258=
ENST00000465635.5:n.229C>A
ENST00000483340.1:n.310C>A
ENST00000620295.2:c.3732C>A	ENSP00000478500.1:p.Ile1244=
ENST00000622724.3:c.3696C>A	ENSP00000480063.1:p.Ile1232=
NM_015074.3:c.3636C>A , LRG_252t1:c.3636C>A	NP_055889.2:p.Ile1212=
NM_001365951.1:c.3774C>A	NP_001352880.1:p.Ile1258=
NM_001365952.1:c.3774C>A	NP_001352881.1:p.Ile1258=
NM_001365951.3:c.3774C>A MANE Select	NP_001352880.1:p.Ile1258=