Canonical Allele Identifier: CA338324018

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10428529T>C (hg19) ; chr1:g.10368471T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10368471T>C , CM000663.2:g.10368471T>C	GRCh38
NC_000001.10:g.10428529T>C , CM000663.1:g.10428529T>C	GRCh37
NC_000001.9:g.10351116T>C	NCBI36
NG_008069.1:g.162766T>C , LRG_252:g.162766T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.4820T>C	ENSP00000512668.1:p.Leu1607Pro
ENST00000696503.1:c.4682T>C	ENSP00000512669.1:p.Leu1561Pro
ENST00000696504.1:c.4682T>C	ENSP00000512670.1:p.Leu1561Pro
ENST00000676179.1:c.4757T>C MANE Select	ENSP00000502065.1:p.Leu1586Pro
ENST00000263934.10:c.4619T>C	ENSP00000263934.6:p.Leu1540Pro
ENST00000377081.5:c.4757T>C	ENSP00000366284.1:p.Leu1586Pro
ENST00000377086.5:c.4757T>C	ENSP00000366290.1:p.Leu1586Pro
ENST00000470616.1:n.488T>C
ENST00000620295.2:c.4715T>C	ENSP00000478500.1:p.Leu1572Pro
ENST00000622724.3:c.4679T>C	ENSP00000480063.1:p.Leu1560Pro
ENST00000635499.1:c.802T>C
NM_015074.3:c.4619T>C , LRG_252t1:c.4619T>C	NP_055889.2:p.Leu1540Pro
NM_001365951.1:c.4757T>C	NP_001352880.1:p.Leu1586Pro
NM_001365952.1:c.4757T>C	NP_001352881.1:p.Leu1586Pro
NM_001365951.3:c.4757T>C MANE Select	NP_001352880.1:p.Leu1586Pro