Canonical Allele Identifier: CA415884346
Gene: KIF1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.10403335G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10343277G>T , CM000663.2:g.10343277G>T GRCh38
NC_000001.10:g.10403335G>T , CM000663.1:g.10403335G>T GRCh37
NC_000001.9:g.10325922G>T NCBI36
NG_008069.1:g.137572G>T , LRG_252:g.137572G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696502.1:c.3540G>T ENSP00000512668.1:p.Leu1180=
ENST00000696503.1:c.3603G>T ENSP00000512669.1:p.Leu1201=
ENST00000696504.1:c.3603G>T ENSP00000512670.1:p.Leu1201=
ENST00000676179.1:c.3678G>T MANE Select ENSP00000502065.1:p.Leu1226=
ENST00000263934.10:c.3540G>T ENSP00000263934.6:p.Leu1180=
ENST00000377081.5:c.3678G>T ENSP00000366284.1:p.Leu1226=
ENST00000377086.5:c.3678G>T ENSP00000366290.1:p.Leu1226=
ENST00000620295.2:c.3636G>T ENSP00000478500.1:p.Leu1212=
ENST00000622724.3:c.3600G>T ENSP00000480063.1:p.Leu1200=
NM_015074.3:c.3540G>T , LRG_252t1:c.3540G>T NP_055889.2:p.Leu1180=
NM_001365951.1:c.3678G>T NP_001352880.1:p.Leu1226=
NM_001365952.1:c.3678G>T NP_001352881.1:p.Leu1226=
NM_001365951.3:c.3678G>T MANE Select NP_001352880.1:p.Leu1226=