Canonical Allele Identifier: CA415881650

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10384829T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10324771T>C , CM000663.2:g.10324771T>C	GRCh38
NC_000001.10:g.10384829T>C , CM000663.1:g.10384829T>C	GRCh37
NC_000001.9:g.10307416T>C	NCBI36
NG_008069.1:g.119066T>C , LRG_252:g.119066T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.2413T>C	ENSP00000512668.1:p.Leu805=
ENST00000696503.1:c.2476T>C	ENSP00000512669.1:p.Leu826=
ENST00000696504.1:c.2476T>C	ENSP00000512670.1:p.Leu826=
ENST00000676179.1:c.2551T>C MANE Select	ENSP00000502065.1:p.Leu851=
ENST00000263934.10:c.2413T>C	ENSP00000263934.6:p.Leu805=
ENST00000377081.5:c.2551T>C	ENSP00000366284.1:p.Leu851=
ENST00000377086.5:c.2551T>C	ENSP00000366290.1:p.Leu851=
ENST00000620295.2:c.2509T>C	ENSP00000478500.1:p.Leu837=
ENST00000622724.3:c.2473T>C	ENSP00000480063.1:p.Leu825=
NM_015074.3:c.2413T>C , LRG_252t1:c.2413T>C	NP_055889.2:p.Leu805=
NM_001365951.1:c.2551T>C	NP_001352880.1:p.Leu851=
NM_001365952.1:c.2551T>C	NP_001352881.1:p.Leu851=
NM_001365951.3:c.2551T>C MANE Select	NP_001352880.1:p.Leu851=