Canonical Allele Identifier: CA801630328

Gene: FBXL17

Linked Data

• dbSNP Id: rs1329961769
• MyVariant Identifiers: chr5:g.107400622_107400623insTTTAGCTTTTTAAA (hg19) ; chr5:g.108064921_108064922insTTTAGCTTTTTAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108064926_108064939dup , CM000667.2:g.108064926_108064939dup	GRCh38
NC_000005.9:g.107400627_107400640dup , CM000667.1:g.107400627_107400640dup	GRCh37
NC_000005.8:g.107428526_107428539dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.754-43934_754-43921dup
ENST00000542267.7:c.1746-43934_1746-43921dup MANE Select	ENSP00000437464.2:n.1746-43934_1746-43921dup
ENST00000359660.9:c.552-43934_552-43921dup	ENSP00000352683.4:n.552-43934_552-43921dup
ENST00000481160.1:n.402-43934_402-43921dup
ENST00000496714.1:c.552-43934_552-43921dup	ENSP00000418111.1:n.552-43934_552-43921dup
ENST00000542267.5:c.1746-43934_1746-43921dup	ENSP00000437464.1:n.1746-43934_1746-43921dup
ENST00000619412.4:c.1032-43934_1032-43921dup	ENSP00000481439.1:n.1032-43934_1032-43921dup
NM_001163315.2:c.1746-43934_1746-43921dup	NP_001156787.2:n.1746-43934_1746-43921dup
XM_005272048.3:c.1746-43934_1746-43921dup	XP_005272105.1:n.1746-43934_1746-43921dup
XM_011543574.1:c.1746-43934_1746-43921dup	XP_011541876.1:n.1746-43934_1746-43921dup
XM_011543575.1:c.1746-43934_1746-43921dup	XP_011541877.1:n.1746-43934_1746-43921dup
XM_005272048.4:c.1746-43934_1746-43921dup	XP_005272105.1:n.1746-43934_1746-43921dup
XM_011543574.3:c.1746-43934_1746-43921dup	XP_011541876.1:n.1746-43934_1746-43921dup
XM_011543575.2:c.1746-43934_1746-43921dup	XP_011541877.1:n.1746-43934_1746-43921dup
NM_001163315.3:c.1746-43934_1746-43921dup MANE Select	NP_001156787.2:n.1746-43934_1746-43921dup