Canonical Allele Identifier: CA415886679

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10428539C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368481C>T , CM000663.2:g.10368481C>T	GRCh38
NC_000001.10:g.10428539C>T , CM000663.1:g.10428539C>T	GRCh37
NC_000001.9:g.10351126C>T	NCBI36
NG_008069.1:g.162776C>T , LRG_252:g.162776C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4830C>T	ENSP00000512668.1:p.Leu1610=
ENST00000696503.1:c.4692C>T	ENSP00000512669.1:p.Leu1564=
ENST00000696504.1:c.4692C>T	ENSP00000512670.1:p.Leu1564=
ENST00000676179.1:c.4767C>T MANE Select	ENSP00000502065.1:p.Leu1589=
ENST00000263934.10:c.4629C>T	ENSP00000263934.6:p.Leu1543=
ENST00000377081.5:c.4767C>T	ENSP00000366284.1:p.Leu1589=
ENST00000377086.5:c.4767C>T	ENSP00000366290.1:p.Leu1589=
ENST00000470616.1:n.498C>T
ENST00000620295.2:c.4725C>T	ENSP00000478500.1:p.Leu1575=
ENST00000622724.3:c.4689C>T	ENSP00000480063.1:p.Leu1563=
ENST00000635499.1:c.812C>T
NM_015074.3:c.4629C>T , LRG_252t1:c.4629C>T	NP_055889.2:p.Leu1543=
NM_001365951.1:c.4767C>T	NP_001352880.1:p.Leu1589=
NM_001365952.1:c.4767C>T	NP_001352881.1:p.Leu1589=
NM_001365951.3:c.4767C>T MANE Select	NP_001352880.1:p.Leu1589=