Canonical Allele Identifier: CA1571062847
Gene: FBXL17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.108064959_108064960delinsTA , CM000667.2:g.108064959_108064960delinsTA GRCh38
NC_000005.9:g.107400660_107400661delinsTA , CM000667.1:g.107400660_107400661delinsTA GRCh37
NC_000005.8:g.107428559_107428560delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496714.2:c.754-43959_754-43958delinsTA
ENST00000542267.7:c.1746-43959_1746-43958delinsTA MANE Select ENSP00000437464.2:n.1746-43959_1746-43958delinsTA
ENST00000359660.9:c.552-43959_552-43958delinsTA ENSP00000352683.4:n.552-43959_552-43958delinsTA
ENST00000481160.1:n.402-43959_402-43958delinsTA
ENST00000496714.1:c.552-43959_552-43958delinsTA ENSP00000418111.1:n.552-43959_552-43958delinsTA
ENST00000542267.5:c.1746-43959_1746-43958delinsTA ENSP00000437464.1:n.1746-43959_1746-43958delinsTA
ENST00000619412.4:c.1032-43959_1032-43958delinsTA ENSP00000481439.1:n.1032-43959_1032-43958delinsTA
NM_001163315.2:c.1746-43959_1746-43958delinsTA NP_001156787.2:n.1746-43959_1746-43958delinsTA
XM_005272048.3:c.1746-43959_1746-43958delinsTA XP_005272105.1:n.1746-43959_1746-43958delinsTA
XM_011543574.1:c.1746-43959_1746-43958delinsTA XP_011541876.1:n.1746-43959_1746-43958delinsTA
XM_011543575.1:c.1746-43959_1746-43958delinsTA XP_011541877.1:n.1746-43959_1746-43958delinsTA
XM_005272048.4:c.1746-43959_1746-43958delinsTA XP_005272105.1:n.1746-43959_1746-43958delinsTA
XM_011543574.3:c.1746-43959_1746-43958delinsTA XP_011541876.1:n.1746-43959_1746-43958delinsTA
XM_011543575.2:c.1746-43959_1746-43958delinsTA XP_011541877.1:n.1746-43959_1746-43958delinsTA
NM_001163315.3:c.1746-43959_1746-43958delinsTA MANE Select NP_001156787.2:n.1746-43959_1746-43958delinsTA