Canonical Allele Identifier: CA581650

Gene: KIF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10334529T>G , CM000663.2:g.10334529T>G	GRCh38
NC_000001.10:g.10394587T>G , CM000663.1:g.10394587T>G	GRCh37
NC_000001.9:g.10317174T>G	NCBI36
NG_008069.1:g.128824T>G , LRG_252:g.128824T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365951.3:c.2934T>G MANE Select	NP_001352880.1:p.Val978=
ENST00000676179.1:c.2934T>G MANE Select	ENSP00000502065.1:p.Val978=
NM_001365951.1:c.2934T>G	NP_001352880.1:p.Val978=
NM_001365952.1:c.2934T>G	NP_001352881.1:p.Val978=
NM_015074.3:c.2796T>G , LRG_252t1:c.2796T>G	NP_055889.2:p.Val932=
ENST00000263934.10:c.2796T>G	ENSP00000263934.6:p.Val932=
ENST00000377081.5:c.2934T>G	ENSP00000366284.1:p.Val978=
ENST00000377086.5:c.2934T>G	ENSP00000366290.1:p.Val978=
ENST00000620295.2:c.2892T>G	ENSP00000478500.1:p.Val964=
ENST00000622724.3:c.2856T>G	ENSP00000480063.1:p.Val952=
ENST00000696502.1:c.2796T>G	ENSP00000512668.1:p.Val932=
ENST00000696503.1:c.2859T>G	ENSP00000512669.1:p.Val953=
ENST00000696504.1:c.2859T>G	ENSP00000512670.1:p.Val953=