Canonical Allele Identifier: CA1571062779

Gene: FBXL17

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108064821_108064865delinsAGCCTTCCTGCAGCTTCCTTCCAGCAGAGGATCTCATCTGGGACG , CM000667.2:g.108064821_108064865delinsAGCCTTCCTGCAGCTTCCTTCCAGCAGAGGATCTCATCTGGGACG	GRCh38
NC_000005.9:g.107400522_107400566delinsAGCCTTCCTGCAGCTTCCTTCCAGCAGAGGATCTCATCTGGGACG , CM000667.1:g.107400522_107400566delinsAGCCTTCCTGCAGCTTCCTTCCAGCAGAGGATCTCATCTGGGACG	GRCh37
NC_000005.8:g.107428421_107428465delinsAGCCTTCCTGCAGCTTCCTTCCAGCAGAGGATCTCATCTGGGACG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.754-43864_754-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT
ENST00000542267.7:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT MANE Select	ENSP00000437464.2:n.1746-43864_1746-43820delinsCGTCCCAGATGAGA...
ENST00000359660.9:c.552-43864_552-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	ENSP00000352683.4:n.552-43864_552-43820delinsCGTCCCAGATGAGATC...
ENST00000481160.1:n.402-43864_402-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT
ENST00000496714.1:c.552-43864_552-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	ENSP00000418111.1:n.552-43864_552-43820delinsCGTCCCAGATGAGATC...
ENST00000542267.5:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	ENSP00000437464.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGA...
ENST00000619412.4:c.1032-43864_1032-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	ENSP00000481439.1:n.1032-43864_1032-43820delinsCGTCCCAGATGAGA...
NM_001163315.2:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	NP_001156787.2:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
XM_005272048.3:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	XP_005272105.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
XM_011543574.1:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	XP_011541876.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
XM_011543575.1:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	XP_011541877.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
XM_005272048.4:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	XP_005272105.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
XM_011543574.3:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	XP_011541876.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
XM_011543575.2:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT	XP_011541877.1:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...
NM_001163315.3:c.1746-43864_1746-43820delinsCGTCCCAGATGAGATCCTCTGCTGGAAGGAAGCTGCAGGAAGGCT MANE Select	NP_001156787.2:n.1746-43864_1746-43820delinsCGTCCCAGATGAGATCC...