Canonical Allele Identifier: CA17845122

Gene: KIF1B

Linked Data

• dbSNP Id: rs771654812
• gnomAD v4: 1-10346002-A-C
• MyVariant Identifiers: chr1:g.10406060A>C (hg19) ; chr1:g.10346002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10346002A>C , CM000663.2:g.10346002A>C	GRCh38
NC_000001.10:g.10406060A>C , CM000663.1:g.10406060A>C	GRCh37
NC_000001.9:g.10328647A>C	NCBI36
NG_008069.1:g.140297A>C , LRG_252:g.140297A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3860+49A>C	ENSP00000512668.1:n.3860+49A>C
ENST00000696503.1:c.3722+49A>C	ENSP00000512669.1:n.3722+49A>C
ENST00000696504.1:c.3722+49A>C	ENSP00000512670.1:n.3722+49A>C
ENST00000676179.1:c.3797+49A>C MANE Select	ENSP00000502065.1:n.3797+49A>C
ENST00000263934.10:c.3659+49A>C	ENSP00000263934.6:n.3659+49A>C
ENST00000377081.5:c.3797+49A>C	ENSP00000366284.1:n.3797+49A>C
ENST00000377086.5:c.3797+49A>C	ENSP00000366290.1:n.3797+49A>C
ENST00000465635.5:n.252+49A>C
ENST00000483340.1:n.333+49A>C
ENST00000620295.2:c.3755+49A>C	ENSP00000478500.1:n.3755+49A>C
ENST00000622724.3:c.3719+49A>C	ENSP00000480063.1:n.3719+49A>C
NM_015074.3:c.3659+49A>C , LRG_252t1:c.3659+49A>C	NP_055889.2:n.3659+49A>C
NM_001365951.1:c.3797+49A>C	NP_001352880.1:n.3797+49A>C
NM_001365952.1:c.3797+49A>C	NP_001352881.1:n.3797+49A>C
NM_001365951.3:c.3797+49A>C MANE Select	NP_001352880.1:n.3797+49A>C