Canonical Allele Identifier: CA2580092715

Gene: FLCN MPRIP

Linked Data

• ClinVar Variation Id: 1769146
• ClinVar RCV Id: RCV002380584

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17216364_17216390del , CM000679.2:g.17216364_17216390del	GRCh38
NC_000017.10:g.17119678_17119704del , CM000679.1:g.17119678_17119704del	GRCh37
NC_000017.9:g.17060403_17060429del	NCBI36
NG_008001.2:g.25802_25828del , LRG_325:g.25802_25828del

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.1293_1300+19del (FLCN)
ENST00000285071.8:c.1293_1300+19del (FLCN)
ENST00000427497.3:c.*127_*134+19del
ENST00000578209.5:c.562-1126_562-1100del (MPRIP)
NM_144997.5:c.1293_1300+19del , LRG_325t1:c.1293_1300+19del (FLCN)
XM_011523714.1:c.1347_1354+19del (FLCN)
XM_011523715.1:c.1347_1354+19del (FLCN)
XM_011523716.1:c.1347_1354+19del (FLCN)
XM_011523717.1:c.1347_1354+19del (FLCN)
XM_011523718.1:c.1347_1354+19del (FLCN)
XM_011523719.1:c.1347_1354+19del (FLCN)
XM_011523720.1:c.1071_1078+19del (FLCN)
XM_011523721.1:c.1347_1354+19del (FLCN)
XR_934007.1:n.2570+682_2570+708del (FLCN)
NM_001353229.1:c.1347_1354+19del (FLCN)
NM_001353230.1:c.1293_1300+19del (FLCN)
NM_001353231.1:c.1293_1300+19del (FLCN)
NM_144997.6:c.1293_1300+19del (FLCN)
XM_011523714.3:c.1347_1354+19del (FLCN)
XM_011523718.3:c.1347_1354+19del (FLCN)
XM_011523719.3:c.1347_1354+19del (FLCN)
XM_011523721.3:c.1347_1354+19del (FLCN)
XM_017024305.2:c.1347_1354+19del (FLCN)
XM_017024308.1:c.1293_1300+19del (FLCN)
XM_017024309.2:c.1071_1078+19del (FLCN)
XM_024450635.1:c.1347_1354+19del (FLCN)
XR_001752445.2:n.1734+682_1734+708del (FLCN)
NM_144997.7:c.1293_1300+19del (FLCN)
NM_001353229.2:c.1347_1354+19del (FLCN)
NM_001353230.2:c.1293_1300+19del (FLCN)
NM_001353231.2:c.1293_1300+19del (FLCN)