Canonical Allele Identifier: CA338343568

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10408729T>C (hg19) ; chr1:g.10348671T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348671T>C , CM000663.2:g.10348671T>C	GRCh38
NC_000001.10:g.10408729T>C , CM000663.1:g.10408729T>C	GRCh37
NC_000001.9:g.10331316T>C	NCBI36
NG_008069.1:g.142966T>C , LRG_252:g.142966T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3950T>C	ENSP00000512668.1:p.Val1317Ala
ENST00000696503.1:c.3812T>C	ENSP00000512669.1:p.Val1271Ala
ENST00000696504.1:c.3812T>C	ENSP00000512670.1:p.Val1271Ala
ENST00000676179.1:c.3887T>C MANE Select	ENSP00000502065.1:p.Val1296Ala
ENST00000263934.10:c.3749T>C	ENSP00000263934.6:p.Val1250Ala
ENST00000377081.5:c.3887T>C	ENSP00000366284.1:p.Val1296Ala
ENST00000377086.5:c.3887T>C	ENSP00000366290.1:p.Val1296Ala
ENST00000465635.5:n.342T>C
ENST00000483340.1:n.423T>C
ENST00000620295.2:c.3845T>C	ENSP00000478500.1:p.Val1282Ala
ENST00000622724.3:c.3809T>C	ENSP00000480063.1:p.Val1270Ala
NM_015074.3:c.3749T>C , LRG_252t1:c.3749T>C	NP_055889.2:p.Val1250Ala
NM_001365951.1:c.3887T>C	NP_001352880.1:p.Val1296Ala
NM_001365952.1:c.3887T>C	NP_001352881.1:p.Val1296Ala
NM_001365951.3:c.3887T>C MANE Select	NP_001352880.1:p.Val1296Ala