Canonical Allele Identifier: CA338340331

Gene: KIF1B

Linked Data

• ClinVar Variation Id: 1728126
• ClinVar RCV Id: RCV003581821 ; RCV004048461
• gnomAD v4: 1-10337395-A-C
• MyVariant Identifiers: chr1:g.10397453A>C (hg19) ; chr1:g.10337395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10337395A>C , CM000663.2:g.10337395A>C	GRCh38
NC_000001.10:g.10397453A>C , CM000663.1:g.10397453A>C	GRCh37
NC_000001.9:g.10320040A>C	NCBI36
NG_008069.1:g.131690A>C , LRG_252:g.131690A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3146A>C	ENSP00000512668.1:p.Asp1049Ala
ENST00000696503.1:c.3209A>C	ENSP00000512669.1:p.Asp1070Ala
ENST00000696504.1:c.3209A>C	ENSP00000512670.1:p.Asp1070Ala
ENST00000676179.1:c.3284A>C MANE Select	ENSP00000502065.1:p.Asp1095Ala
ENST00000263934.10:c.3146A>C	ENSP00000263934.6:p.Asp1049Ala
ENST00000377081.5:c.3284A>C	ENSP00000366284.1:p.Asp1095Ala
ENST00000377086.5:c.3284A>C	ENSP00000366290.1:p.Asp1095Ala
ENST00000620295.2:c.3242A>C	ENSP00000478500.1:p.Asp1081Ala
ENST00000622724.3:c.3206A>C	ENSP00000480063.1:p.Asp1069Ala
NM_015074.3:c.3146A>C , LRG_252t1:c.3146A>C	NP_055889.2:p.Asp1049Ala
NM_001365951.1:c.3284A>C	NP_001352880.1:p.Asp1095Ala
NM_001365952.1:c.3284A>C	NP_001352881.1:p.Asp1095Ala
NM_001365951.3:c.3284A>C MANE Select	NP_001352880.1:p.Asp1095Ala