Canonical Allele Identifier: CA801558947

Gene: FBXL17

Linked Data

• dbSNP Id: rs1449240370
• gnomAD v3: 5-107945820-T-C
• gnomAD v4: 5-107945820-T-C
• MyVariant Identifiers: chr5:g.107281521T>C (hg19) ; chr5:g.107945820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.107945820T>C , CM000667.2:g.107945820T>C	GRCh38
NC_000005.9:g.107281521T>C , CM000667.1:g.107281521T>C	GRCh37
NC_000005.8:g.107309420T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000496714.2:c.831-64641A>G
ENST00000542267.7:c.1823-64641A>G MANE Select	ENSP00000437464.2:n.1823-64641A>G
ENST00000359660.9:c.629-64641A>G	ENSP00000352683.4:n.629-64641A>G
ENST00000496714.1:c.629-64641A>G	ENSP00000418111.1:n.629-64641A>G
ENST00000542267.5:c.1823-64641A>G	ENSP00000437464.1:n.1823-64641A>G
ENST00000619412.4:c.1109-64641A>G	ENSP00000481439.1:n.1109-64641A>G
NM_001163315.2:c.1823-64641A>G	NP_001156787.2:n.1823-64641A>G
XM_005272048.3:c.1823-64641A>G	XP_005272105.1:n.1823-64641A>G
XM_005272048.4:c.1823-64641A>G	XP_005272105.1:n.1823-64641A>G
NM_001163315.3:c.1823-64641A>G MANE Select	NP_001156787.2:n.1823-64641A>G