Canonical Allele Identifier: CA338321996

Gene: KIF1B

Linked Data

• dbSNP Id: rs1569908621
• MyVariant Identifiers: chr1:g.10425545T>A (hg19) ; chr1:g.10365487T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365487T>A , CM000663.2:g.10365487T>A	GRCh38
NC_000001.10:g.10425545T>A , CM000663.1:g.10425545T>A	GRCh37
NC_000001.9:g.10348132T>A	NCBI36
NG_008069.1:g.159782T>A , LRG_252:g.159782T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4654T>A	ENSP00000512668.1:p.Ser1552Thr
ENST00000696503.1:c.4516T>A	ENSP00000512669.1:p.Ser1506Thr
ENST00000696504.1:c.4516T>A	ENSP00000512670.1:p.Ser1506Thr
ENST00000676179.1:c.4591T>A MANE Select	ENSP00000502065.1:p.Ser1531Thr
ENST00000263934.10:c.4453T>A	ENSP00000263934.6:p.Ser1485Thr
ENST00000377081.5:c.4591T>A	ENSP00000366284.1:p.Ser1531Thr
ENST00000377086.5:c.4591T>A	ENSP00000366290.1:p.Ser1531Thr
ENST00000470616.1:n.322T>A
ENST00000620295.2:c.4549T>A	ENSP00000478500.1:p.Ser1517Thr
ENST00000622724.3:c.4513T>A	ENSP00000480063.1:p.Ser1505Thr
ENST00000635499.1:c.636T>A
NM_015074.3:c.4453T>A , LRG_252t1:c.4453T>A	NP_055889.2:p.Ser1485Thr
XR_946953.1:n.355+894A>T
NM_001365951.1:c.4591T>A	NP_001352880.1:p.Ser1531Thr
NM_001365952.1:c.4591T>A	NP_001352881.1:p.Ser1531Thr
XR_946953.2:n.230+894A>T
NM_001365951.3:c.4591T>A MANE Select	NP_001352880.1:p.Ser1531Thr