Canonical Allele Identifier: CA1571062835

Gene: FBXL17

Linked Data

• dbSNP Id: rs1748060733

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108064935_108064940del , CM000667.2:g.108064935_108064940del	GRCh38
NC_000005.9:g.107400636_107400641del , CM000667.1:g.107400636_107400641del	GRCh37
NC_000005.8:g.107428535_107428540del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.754-43934_754-43929del
ENST00000542267.7:c.1746-43934_1746-43929del MANE Select	ENSP00000437464.2:n.1746-43934_1746-43929del
ENST00000359660.9:c.552-43934_552-43929del	ENSP00000352683.4:n.552-43934_552-43929del
ENST00000481160.1:n.402-43934_402-43929del
ENST00000496714.1:c.552-43934_552-43929del	ENSP00000418111.1:n.552-43934_552-43929del
ENST00000542267.5:c.1746-43934_1746-43929del	ENSP00000437464.1:n.1746-43934_1746-43929del
ENST00000619412.4:c.1032-43934_1032-43929del	ENSP00000481439.1:n.1032-43934_1032-43929del
NM_001163315.2:c.1746-43934_1746-43929del	NP_001156787.2:n.1746-43934_1746-43929del
XM_005272048.3:c.1746-43934_1746-43929del	XP_005272105.1:n.1746-43934_1746-43929del
XM_011543574.1:c.1746-43934_1746-43929del	XP_011541876.1:n.1746-43934_1746-43929del
XM_011543575.1:c.1746-43934_1746-43929del	XP_011541877.1:n.1746-43934_1746-43929del
XM_005272048.4:c.1746-43934_1746-43929del	XP_005272105.1:n.1746-43934_1746-43929del
XM_011543574.3:c.1746-43934_1746-43929del	XP_011541876.1:n.1746-43934_1746-43929del
XM_011543575.2:c.1746-43934_1746-43929del	XP_011541877.1:n.1746-43934_1746-43929del
NM_001163315.3:c.1746-43934_1746-43929del MANE Select	NP_001156787.2:n.1746-43934_1746-43929del