Canonical Allele Identifier: CA2541816476

Gene: FBXL17

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108064860G>T , CM000667.2:g.108064860G>T	GRCh38
NC_000005.9:g.107400561G>T , CM000667.1:g.107400561G>T	GRCh37
NC_000005.8:g.107428460G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.754-43859C>A
ENST00000542267.7:c.1746-43859C>A MANE Select	ENSP00000437464.2:n.1746-43859C>A
ENST00000359660.9:c.552-43859C>A	ENSP00000352683.4:n.552-43859C>A
ENST00000481160.1:n.402-43859C>A
ENST00000496714.1:c.552-43859C>A	ENSP00000418111.1:n.552-43859C>A
ENST00000542267.5:c.1746-43859C>A	ENSP00000437464.1:n.1746-43859C>A
ENST00000619412.4:c.1032-43859C>A	ENSP00000481439.1:n.1032-43859C>A
NM_001163315.2:c.1746-43859C>A	NP_001156787.2:n.1746-43859C>A
XM_005272048.3:c.1746-43859C>A	XP_005272105.1:n.1746-43859C>A
XM_011543574.1:c.1746-43859C>A	XP_011541876.1:n.1746-43859C>A
XM_011543575.1:c.1746-43859C>A	XP_011541877.1:n.1746-43859C>A
XM_005272048.4:c.1746-43859C>A	XP_005272105.1:n.1746-43859C>A
XM_011543574.3:c.1746-43859C>A	XP_011541876.1:n.1746-43859C>A
XM_011543575.2:c.1746-43859C>A	XP_011541877.1:n.1746-43859C>A
NM_001163315.3:c.1746-43859C>A MANE Select	NP_001156787.2:n.1746-43859C>A