Canonical Allele Identifier: CA1571062772
Gene: FBXL17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.108064806_108064807delinsCT , CM000667.2:g.108064806_108064807delinsCT GRCh38
NC_000005.9:g.107400507_107400508delinsCT , CM000667.1:g.107400507_107400508delinsCT GRCh37
NC_000005.8:g.107428406_107428407delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496714.2:c.754-43806_754-43805delinsAG
ENST00000542267.7:c.1746-43806_1746-43805delinsAG MANE Select ENSP00000437464.2:n.1746-43806_1746-43805delinsAG
ENST00000359660.9:c.552-43806_552-43805delinsAG ENSP00000352683.4:n.552-43806_552-43805delinsAG
ENST00000481160.1:n.402-43806_402-43805delinsAG
ENST00000496714.1:c.552-43806_552-43805delinsAG ENSP00000418111.1:n.552-43806_552-43805delinsAG
ENST00000542267.5:c.1746-43806_1746-43805delinsAG ENSP00000437464.1:n.1746-43806_1746-43805delinsAG
ENST00000619412.4:c.1032-43806_1032-43805delinsAG ENSP00000481439.1:n.1032-43806_1032-43805delinsAG
NM_001163315.2:c.1746-43806_1746-43805delinsAG NP_001156787.2:n.1746-43806_1746-43805delinsAG
XM_005272048.3:c.1746-43806_1746-43805delinsAG XP_005272105.1:n.1746-43806_1746-43805delinsAG
XM_011543574.1:c.1746-43806_1746-43805delinsAG XP_011541876.1:n.1746-43806_1746-43805delinsAG
XM_011543575.1:c.1746-43806_1746-43805delinsAG XP_011541877.1:n.1746-43806_1746-43805delinsAG
XM_005272048.4:c.1746-43806_1746-43805delinsAG XP_005272105.1:n.1746-43806_1746-43805delinsAG
XM_011543574.3:c.1746-43806_1746-43805delinsAG XP_011541876.1:n.1746-43806_1746-43805delinsAG
XM_011543575.2:c.1746-43806_1746-43805delinsAG XP_011541877.1:n.1746-43806_1746-43805delinsAG
NM_001163315.3:c.1746-43806_1746-43805delinsAG MANE Select NP_001156787.2:n.1746-43806_1746-43805delinsAG