Canonical Allele Identifier: CA415881683

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10384900G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324842G>C , CM000663.2:g.10324842G>C	GRCh38
NC_000001.10:g.10384900G>C , CM000663.1:g.10384900G>C	GRCh37
NC_000001.9:g.10307487G>C	NCBI36
NG_008069.1:g.119137G>C , LRG_252:g.119137G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.2484G>C	ENSP00000512668.1:p.Val828=
ENST00000696503.1:c.2547G>C	ENSP00000512669.1:p.Val849=
ENST00000696504.1:c.2547G>C	ENSP00000512670.1:p.Val849=
ENST00000676179.1:c.2622G>C MANE Select	ENSP00000502065.1:p.Val874=
ENST00000263934.10:c.2484G>C	ENSP00000263934.6:p.Val828=
ENST00000377081.5:c.2622G>C	ENSP00000366284.1:p.Val874=
ENST00000377086.5:c.2622G>C	ENSP00000366290.1:p.Val874=
ENST00000620295.2:c.2580G>C	ENSP00000478500.1:p.Val860=
ENST00000622724.3:c.2544G>C	ENSP00000480063.1:p.Val848=
NM_015074.3:c.2484G>C , LRG_252t1:c.2484G>C	NP_055889.2:p.Val828=
NM_001365951.1:c.2622G>C	NP_001352880.1:p.Val874=
NM_001365952.1:c.2622G>C	NP_001352881.1:p.Val874=
NM_001365951.3:c.2622G>C MANE Select	NP_001352880.1:p.Val874=