Canonical Allele Identifier: CA1571062778

Gene: FBXL17

Linked Data

• dbSNP Id: rs1409640278

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108064812A>G , CM000667.2:g.108064812A>G	GRCh38
NC_000005.9:g.107400513A>G , CM000667.1:g.107400513A>G	GRCh37
NC_000005.8:g.107428412A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.754-43811T>C
ENST00000542267.7:c.1746-43811T>C MANE Select	ENSP00000437464.2:n.1746-43811T>C
ENST00000359660.9:c.552-43811T>C	ENSP00000352683.4:n.552-43811T>C
ENST00000481160.1:n.402-43811T>C
ENST00000496714.1:c.552-43811T>C	ENSP00000418111.1:n.552-43811T>C
ENST00000542267.5:c.1746-43811T>C	ENSP00000437464.1:n.1746-43811T>C
ENST00000619412.4:c.1032-43811T>C	ENSP00000481439.1:n.1032-43811T>C
NM_001163315.2:c.1746-43811T>C	NP_001156787.2:n.1746-43811T>C
XM_005272048.3:c.1746-43811T>C	XP_005272105.1:n.1746-43811T>C
XM_011543574.1:c.1746-43811T>C	XP_011541876.1:n.1746-43811T>C
XM_011543575.1:c.1746-43811T>C	XP_011541877.1:n.1746-43811T>C
XM_005272048.4:c.1746-43811T>C	XP_005272105.1:n.1746-43811T>C
XM_011543574.3:c.1746-43811T>C	XP_011541876.1:n.1746-43811T>C
XM_011543575.2:c.1746-43811T>C	XP_011541877.1:n.1746-43811T>C
NM_001163315.3:c.1746-43811T>C MANE Select	NP_001156787.2:n.1746-43811T>C