Canonical Allele Identifier: CA338315548

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10356657C>G (hg19) ; chr1:g.10296599C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10296599C>G , CM000663.2:g.10296599C>G	GRCh38
NC_000001.10:g.10356657C>G , CM000663.1:g.10356657C>G	GRCh37
NC_000001.9:g.10279244C>G	NCBI36
NG_008069.1:g.90894C>G , LRG_252:g.90894C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696500.1:c.*829C>G	ENSP00000512666.1:n.*829C>G
ENST00000696502.1:c.1657C>G	ENSP00000512668.1:p.Pro553Ala
ENST00000696503.1:c.1720C>G	ENSP00000512669.1:p.Pro574Ala
ENST00000696504.1:c.1720C>G	ENSP00000512670.1:p.Pro574Ala
ENST00000377093.9:c.1657C>G	ENSP00000366297.4:p.Pro553Ala
ENST00000676179.1:c.1795C>G MANE Select	ENSP00000502065.1:p.Pro599Ala
ENST00000263934.10:c.1657C>G	ENSP00000263934.6:p.Pro553Ala
ENST00000377081.5:c.1795C>G	ENSP00000366284.1:p.Pro599Ala
ENST00000377083.5:c.1657C>G	ENSP00000366287.1:p.Pro553Ala
ENST00000377086.5:c.1795C>G	ENSP00000366290.1:p.Pro599Ala
ENST00000377093.8:c.1657C>G	ENSP00000366297.4:p.Pro553Ala
ENST00000620295.2:c.1753C>G	ENSP00000478500.1:p.Pro585Ala
ENST00000622724.3:c.1717C>G	ENSP00000480063.1:p.Pro573Ala
NM_015074.3:c.1657C>G , LRG_252t1:c.1657C>G	NP_055889.2:p.Pro553Ala
NM_183416.3:c.1657C>G	NP_904325.2:p.Pro553Ala
NM_001365951.1:c.1795C>G	NP_001352880.1:p.Pro599Ala
NM_001365952.1:c.1795C>G	NP_001352881.1:p.Pro599Ala
NM_001365953.1:c.1657C>G	NP_001352882.1:p.Pro553Ala
NM_001365951.3:c.1795C>G MANE Select	NP_001352880.1:p.Pro599Ala
NM_183416.4:c.1657C>G	NP_904325.2:p.Pro553Ala