Canonical Allele Identifier: CA581889
Community Standard Title: NM_001365951.3(KIF1B):c.3813G>A (p.Val1271=)
Gene: KIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10347776G>A , CM000663.2:g.10347776G>A GRCh38
NC_000001.10:g.10407834G>A , CM000663.1:g.10407834G>A GRCh37
NC_000001.9:g.10330421G>A NCBI36
NG_008069.1:g.142071G>A , LRG_252:g.142071G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001365951.3:c.3813G>A MANE Select NP_001352880.1:p.Val1271=
ENST00000676179.1:c.3813G>A MANE Select ENSP00000502065.1:p.Val1271=
NM_001365951.1:c.3813G>A NP_001352880.1:p.Val1271=
NM_001365952.1:c.3813G>A NP_001352881.1:p.Val1271=
NM_015074.3:c.3675G>A , LRG_252t1:c.3675G>A NP_055889.2:p.Val1225=
ENST00000263934.10:c.3675G>A ENSP00000263934.6:p.Val1225=
ENST00000377081.5:c.3813G>A ENSP00000366284.1:p.Val1271=
ENST00000377086.5:c.3813G>A ENSP00000366290.1:p.Val1271=
ENST00000465635.5:n.268G>A
ENST00000483340.1:n.349G>A
ENST00000620295.2:c.3771G>A ENSP00000478500.1:p.Val1257=
ENST00000622724.3:c.3735G>A ENSP00000480063.1:p.Val1245=
ENST00000696502.1:c.3876G>A ENSP00000512668.1:p.Val1292=
ENST00000696503.1:c.3738G>A ENSP00000512669.1:p.Val1246=
ENST00000696504.1:c.3738G>A ENSP00000512670.1:p.Val1246=