Canonical Allele Identifier: CA338343565

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10408728G>T (hg19) ; chr1:g.10348670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348670G>T , CM000663.2:g.10348670G>T	GRCh38
NC_000001.10:g.10408728G>T , CM000663.1:g.10408728G>T	GRCh37
NC_000001.9:g.10331315G>T	NCBI36
NG_008069.1:g.142965G>T , LRG_252:g.142965G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3949G>T	ENSP00000512668.1:p.Val1317Leu
ENST00000696503.1:c.3811G>T	ENSP00000512669.1:p.Val1271Leu
ENST00000696504.1:c.3811G>T	ENSP00000512670.1:p.Val1271Leu
ENST00000676179.1:c.3886G>T MANE Select	ENSP00000502065.1:p.Val1296Leu
ENST00000263934.10:c.3748G>T	ENSP00000263934.6:p.Val1250Leu
ENST00000377081.5:c.3886G>T	ENSP00000366284.1:p.Val1296Leu
ENST00000377086.5:c.3886G>T	ENSP00000366290.1:p.Val1296Leu
ENST00000465635.5:n.341G>T
ENST00000483340.1:n.422G>T
ENST00000620295.2:c.3844G>T	ENSP00000478500.1:p.Val1282Leu
ENST00000622724.3:c.3808G>T	ENSP00000480063.1:p.Val1270Leu
NM_015074.3:c.3748G>T , LRG_252t1:c.3748G>T	NP_055889.2:p.Val1250Leu
NM_001365951.1:c.3886G>T	NP_001352880.1:p.Val1296Leu
NM_001365952.1:c.3886G>T	NP_001352881.1:p.Val1296Leu
NM_001365951.3:c.3886G>T MANE Select	NP_001352880.1:p.Val1296Leu