Canonical Allele Identifier: CA801558967

Gene: FBXL17

Linked Data

• dbSNP Id: rs1212197271
• gnomAD v3: 5-107945886-AT-A
• gnomAD v4: 5-107945886-AT-A
• MyVariant Identifiers: chr5:g.107281588del (hg19) ; chr5:g.107945887del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.107945890del , CM000667.2:g.107945890del	GRCh38
NC_000005.9:g.107281591del , CM000667.1:g.107281591del	GRCh37
NC_000005.8:g.107309490del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000496714.2:c.831-64708del
ENST00000542267.7:c.1823-64708del MANE Select	ENSP00000437464.2:n.1823-64708del
ENST00000359660.9:c.629-64708del	ENSP00000352683.4:n.629-64708del
ENST00000496714.1:c.629-64708del	ENSP00000418111.1:n.629-64708del
ENST00000542267.5:c.1823-64708del	ENSP00000437464.1:n.1823-64708del
ENST00000619412.4:c.1109-64708del	ENSP00000481439.1:n.1109-64708del
NM_001163315.2:c.1823-64708del	NP_001156787.2:n.1823-64708del
XM_005272048.3:c.1823-64708del	XP_005272105.1:n.1823-64708del
XM_005272048.4:c.1823-64708del	XP_005272105.1:n.1823-64708del
NM_001163315.3:c.1823-64708del MANE Select	NP_001156787.2:n.1823-64708del