Canonical Allele Identifier: CA415885351

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10408736T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348678T>A , CM000663.2:g.10348678T>A	GRCh38
NC_000001.10:g.10408736T>A , CM000663.1:g.10408736T>A	GRCh37
NC_000001.9:g.10331323T>A	NCBI36
NG_008069.1:g.142973T>A , LRG_252:g.142973T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3957T>A	ENSP00000512668.1:p.Ile1319=
ENST00000696503.1:c.3819T>A	ENSP00000512669.1:p.Ile1273=
ENST00000696504.1:c.3819T>A	ENSP00000512670.1:p.Ile1273=
ENST00000676179.1:c.3894T>A MANE Select	ENSP00000502065.1:p.Ile1298=
ENST00000263934.10:c.3756T>A	ENSP00000263934.6:p.Ile1252=
ENST00000377081.5:c.3894T>A	ENSP00000366284.1:p.Ile1298=
ENST00000377086.5:c.3894T>A	ENSP00000366290.1:p.Ile1298=
ENST00000465635.5:n.349T>A
ENST00000483340.1:n.430T>A
ENST00000620295.2:c.3852T>A	ENSP00000478500.1:p.Ile1284=
ENST00000622724.3:c.3816T>A	ENSP00000480063.1:p.Ile1272=
NM_015074.3:c.3756T>A , LRG_252t1:c.3756T>A	NP_055889.2:p.Ile1252=
NM_001365951.1:c.3894T>A	NP_001352880.1:p.Ile1298=
NM_001365952.1:c.3894T>A	NP_001352881.1:p.Ile1298=
NM_001365951.3:c.3894T>A MANE Select	NP_001352880.1:p.Ile1298=