Canonical Allele Identifier: CA582208

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10371160T>C , CM000663.2:g.10371160T>C	GRCh38
NC_000001.10:g.10431218T>C , CM000663.1:g.10431218T>C	GRCh37
NC_000001.9:g.10353805T>C	NCBI36
NG_008069.1:g.165455T>C , LRG_252:g.165455T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4844T>C MANE Select	NP_001352880.1:p.Ile1615Thr
ENST00000676179.1:c.4844T>C MANE Select	ENSP00000502065.1:p.Ile1615Thr
NM_001365951.1:c.4844T>C	NP_001352880.1:p.Ile1615Thr
NM_001365952.1:c.4844T>C	NP_001352881.1:p.Ile1615Thr
NM_015074.3:c.4706T>C , LRG_252t1:c.4706T>C	NP_055889.2:p.Ile1569Thr
ENST00000263934.10:c.4706T>C	ENSP00000263934.6:p.Ile1569Thr
ENST00000377081.5:c.4844T>C	ENSP00000366284.1:p.Ile1615Thr
ENST00000377086.5:c.4844T>C	ENSP00000366290.1:p.Ile1615Thr
ENST00000620295.2:c.4802T>C	ENSP00000478500.1:p.Ile1601Thr
ENST00000622724.3:c.4766T>C	ENSP00000480063.1:p.Ile1589Thr
ENST00000635499.1:c.889T>C
ENST00000696502.1:c.4907T>C	ENSP00000512668.1:p.Ile1636Thr
ENST00000696503.1:c.4769T>C	ENSP00000512669.1:p.Ile1590Thr
ENST00000696504.1:c.4769T>C	ENSP00000512670.1:p.Ile1590Thr