Canonical Allele Identifier: CA2580617682

Gene: FLCN MPRIP

Linked Data

• ClinVar Variation Id: 2578491
• ClinVar RCV Id: RCV003326267

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217182_17217194del , CM000679.2:g.17217182_17217194del	GRCh38
NC_000017.10:g.17120496_17120508del , CM000679.1:g.17120496_17120508del	GRCh37
NC_000017.9:g.17061221_17061233del	NCBI36
NG_008001.2:g.24997_25009del , LRG_325:g.24997_25009del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1063-10_1065del (FLCN)
ENST00000285071.8:c.1063-10_1065del (FLCN)
ENST00000427497.3:c.185-10_187del
ENST00000577591.1:n.86-10_88del (FLCN)
ENST00000578209.5:c.562-308_562-296del (MPRIP)
NM_144997.5:c.1063-10_1065del , LRG_325t1:c.1063-10_1065del (FLCN)
XM_011523714.1:c.1117-10_1119del (FLCN)
XM_011523715.1:c.1117-10_1119del (FLCN)
XM_011523716.1:c.1117-10_1119del (FLCN)
XM_011523717.1:c.1117-10_1119del (FLCN)
XM_011523718.1:c.1117-10_1119del (FLCN)
XM_011523719.1:c.1117-10_1119del (FLCN)
XM_011523720.1:c.841-10_843del (FLCN)
XM_011523721.1:c.1117-10_1119del (FLCN)
XR_934007.1:n.2457-10_2459del (FLCN)
NM_001353229.1:c.1117-10_1119del (FLCN)
NM_001353230.1:c.1063-10_1065del (FLCN)
NM_001353231.1:c.1063-10_1065del (FLCN)
NM_144997.6:c.1063-10_1065del (FLCN)
XM_011523714.3:c.1117-10_1119del (FLCN)
XM_011523718.3:c.1117-10_1119del (FLCN)
XM_011523719.3:c.1117-10_1119del (FLCN)
XM_011523721.3:c.1117-10_1119del (FLCN)
XM_017024305.2:c.1117-10_1119del (FLCN)
XM_017024308.1:c.1063-10_1065del (FLCN)
XM_017024309.2:c.841-10_843del (FLCN)
XM_024450635.1:c.1117-10_1119del (FLCN)
XR_001752445.2:n.1621-10_1623del (FLCN)
NM_144997.7:c.1063-10_1065del (FLCN)
NM_001353229.2:c.1117-10_1119del (FLCN)
NM_001353230.2:c.1063-10_1065del (FLCN)
NM_001353231.2:c.1063-10_1065del (FLCN)