Canonical Allele Identifier: CA338342315

Gene: KIF1B

Linked Data

• dbSNP Id: rs1291313452
• gnomAD v4: 1-10345870-G-A
• MyVariant Identifiers: chr1:g.10405928G>A (hg19) ; chr1:g.10345870G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345870G>A , CM000663.2:g.10345870G>A	GRCh38
NC_000001.10:g.10405928G>A , CM000663.1:g.10405928G>A	GRCh37
NC_000001.9:g.10328515G>A	NCBI36
NG_008069.1:g.140165G>A , LRG_252:g.140165G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3777G>A	ENSP00000512668.1:p.Met1259Ile
ENST00000696503.1:c.3639G>A	ENSP00000512669.1:p.Met1213Ile
ENST00000696504.1:c.3639G>A	ENSP00000512670.1:p.Met1213Ile
ENST00000676179.1:c.3714G>A MANE Select	ENSP00000502065.1:p.Met1238Ile
ENST00000263934.10:c.3576G>A	ENSP00000263934.6:p.Met1192Ile
ENST00000377081.5:c.3714G>A	ENSP00000366284.1:p.Met1238Ile
ENST00000377086.5:c.3714G>A	ENSP00000366290.1:p.Met1238Ile
ENST00000465635.5:n.169G>A
ENST00000483340.1:n.250G>A
ENST00000620295.2:c.3672G>A	ENSP00000478500.1:p.Met1224Ile
ENST00000622724.3:c.3636G>A	ENSP00000480063.1:p.Met1212Ile
NM_015074.3:c.3576G>A , LRG_252t1:c.3576G>A	NP_055889.2:p.Met1192Ile
NM_001365951.1:c.3714G>A	NP_001352880.1:p.Met1238Ile
NM_001365952.1:c.3714G>A	NP_001352881.1:p.Met1238Ile
NM_001365951.3:c.3714G>A MANE Select	NP_001352880.1:p.Met1238Ile