Canonical Allele Identifier: CA124766522

Gene: FBXL17

Linked Data

• dbSNP Id: rs916680567
• MyVariant Identifiers: chr5:g.107400513_107400516del (hg19) ; chr5:g.108064812_108064815del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108064814_108064817del , CM000667.2:g.108064814_108064817del	GRCh38
NC_000005.9:g.107400515_107400518del , CM000667.1:g.107400515_107400518del	GRCh37
NC_000005.8:g.107428414_107428417del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496714.2:c.754-43814_754-43811del
ENST00000542267.7:c.1746-43814_1746-43811del MANE Select	ENSP00000437464.2:n.1746-43814_1746-43811del
ENST00000359660.9:c.552-43814_552-43811del	ENSP00000352683.4:n.552-43814_552-43811del
ENST00000481160.1:n.402-43814_402-43811del
ENST00000496714.1:c.552-43814_552-43811del	ENSP00000418111.1:n.552-43814_552-43811del
ENST00000542267.5:c.1746-43814_1746-43811del	ENSP00000437464.1:n.1746-43814_1746-43811del
ENST00000619412.4:c.1032-43814_1032-43811del	ENSP00000481439.1:n.1032-43814_1032-43811del
NM_001163315.2:c.1746-43814_1746-43811del	NP_001156787.2:n.1746-43814_1746-43811del
XM_005272048.3:c.1746-43814_1746-43811del	XP_005272105.1:n.1746-43814_1746-43811del
XM_011543574.1:c.1746-43814_1746-43811del	XP_011541876.1:n.1746-43814_1746-43811del
XM_011543575.1:c.1746-43814_1746-43811del	XP_011541877.1:n.1746-43814_1746-43811del
XM_005272048.4:c.1746-43814_1746-43811del	XP_005272105.1:n.1746-43814_1746-43811del
XM_011543574.3:c.1746-43814_1746-43811del	XP_011541876.1:n.1746-43814_1746-43811del
XM_011543575.2:c.1746-43814_1746-43811del	XP_011541877.1:n.1746-43814_1746-43811del
NM_001163315.3:c.1746-43814_1746-43811del MANE Select	NP_001156787.2:n.1746-43814_1746-43811del