Canonical Allele Identifier: CA415886644

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10428530G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368472G>C , CM000663.2:g.10368472G>C	GRCh38
NC_000001.10:g.10428530G>C , CM000663.1:g.10428530G>C	GRCh37
NC_000001.9:g.10351117G>C	NCBI36
NG_008069.1:g.162767G>C , LRG_252:g.162767G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4821G>C	ENSP00000512668.1:p.Leu1607=
ENST00000696503.1:c.4683G>C	ENSP00000512669.1:p.Leu1561=
ENST00000696504.1:c.4683G>C	ENSP00000512670.1:p.Leu1561=
ENST00000676179.1:c.4758G>C MANE Select	ENSP00000502065.1:p.Leu1586=
ENST00000263934.10:c.4620G>C	ENSP00000263934.6:p.Leu1540=
ENST00000377081.5:c.4758G>C	ENSP00000366284.1:p.Leu1586=
ENST00000377086.5:c.4758G>C	ENSP00000366290.1:p.Leu1586=
ENST00000470616.1:n.489G>C
ENST00000620295.2:c.4716G>C	ENSP00000478500.1:p.Leu1572=
ENST00000622724.3:c.4680G>C	ENSP00000480063.1:p.Leu1560=
ENST00000635499.1:c.803G>C
NM_015074.3:c.4620G>C , LRG_252t1:c.4620G>C	NP_055889.2:p.Leu1540=
NM_001365951.1:c.4758G>C	NP_001352880.1:p.Leu1586=
NM_001365952.1:c.4758G>C	NP_001352881.1:p.Leu1586=
NM_001365951.3:c.4758G>C MANE Select	NP_001352880.1:p.Leu1586=