Canonical Allele Identifier: CA16237514
Gene: FBXL17 HGNC NCBI

Linked Data

dbSNP Id: rs288139

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.108064804G>A , CM000667.2:g.108064804G>A GRCh38
NC_000005.9:g.107400505G>A , CM000667.1:g.107400505G>A GRCh37
NC_000005.8:g.107428404G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000496714.2:c.754-43803C>T
ENST00000542267.7:c.1746-43803C>T MANE Select ENSP00000437464.2:n.1746-43803C>T
ENST00000359660.9:c.552-43803C>T ENSP00000352683.4:n.552-43803C>T
ENST00000481160.1:n.402-43803C>T
ENST00000496714.1:c.552-43803C>T ENSP00000418111.1:n.552-43803C>T
ENST00000542267.5:c.1746-43803C>T ENSP00000437464.1:n.1746-43803C>T
ENST00000619412.4:c.1032-43803C>T ENSP00000481439.1:n.1032-43803C>T
NM_001163315.2:c.1746-43803C>T NP_001156787.2:n.1746-43803C>T
XM_005272048.3:c.1746-43803C>T XP_005272105.1:n.1746-43803C>T
XM_011543574.1:c.1746-43803C>T XP_011541876.1:n.1746-43803C>T
XM_011543575.1:c.1746-43803C>T XP_011541877.1:n.1746-43803C>T
XM_005272048.4:c.1746-43803C>T XP_005272105.1:n.1746-43803C>T
XM_011543574.3:c.1746-43803C>T XP_011541876.1:n.1746-43803C>T
XM_011543575.2:c.1746-43803C>T XP_011541877.1:n.1746-43803C>T
NM_001163315.3:c.1746-43803C>T MANE Select NP_001156787.2:n.1746-43803C>T