Canonical Allele Identifier: CA338327433

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10371180T>C , CM000663.2:g.10371180T>C	GRCh38
NC_000001.10:g.10431238T>C , CM000663.1:g.10431238T>C	GRCh37
NC_000001.9:g.10353825T>C	NCBI36
NG_008069.1:g.165475T>C , LRG_252:g.165475T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.4864T>C MANE Select	NP_001352880.1:p.Ser1622Pro
ENST00000676179.1:c.4864T>C MANE Select	ENSP00000502065.1:p.Ser1622Pro
NM_001365951.1:c.4864T>C	NP_001352880.1:p.Ser1622Pro
NM_001365952.1:c.4864T>C	NP_001352881.1:p.Ser1622Pro
NM_015074.3:c.4726T>C , LRG_252t1:c.4726T>C	NP_055889.2:p.Ser1576Pro
ENST00000263934.10:c.4726T>C	ENSP00000263934.6:p.Ser1576Pro
ENST00000377081.5:c.4864T>C	ENSP00000366284.1:p.Ser1622Pro
ENST00000377086.5:c.4864T>C	ENSP00000366290.1:p.Ser1622Pro
ENST00000620295.2:c.4822T>C	ENSP00000478500.1:p.Ser1608Pro
ENST00000622724.3:c.4786T>C	ENSP00000480063.1:p.Ser1596Pro
ENST00000635499.1:c.909T>C
ENST00000696502.1:c.4927T>C	ENSP00000512668.1:p.Ser1643Pro
ENST00000696503.1:c.4789T>C	ENSP00000512669.1:p.Ser1597Pro
ENST00000696504.1:c.4789T>C	ENSP00000512670.1:p.Ser1597Pro