Canonical Allele Identifier: CA2825002467

Gene: FLCN MPRIP

Linked Data

• ClinVar Variation Id: 3229239
• ClinVar RCV Id: RCV004524818

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17213666_17213672delinsGCTGTGG , CM000679.2:g.17213666_17213672delinsGCTGTGG	GRCh38
NC_000017.10:g.17116980_17116986delinsGCTGTGG , CM000679.1:g.17116980_17116986delinsGCTGTGG	GRCh37
NC_000017.9:g.17057705_17057711delinsGCTGTGG	NCBI36
NG_008001.2:g.28517_28523delinsCCACAGC , LRG_325:g.28517_28523delinsCCACAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1723_1729delinsCCACAGC (FLCN) MANE Select	ENSP00000285071.4:p.Ser575_Ser577delinsProGlnPro
ENST00000285071.8:c.1723_1729delinsCCACAGC (FLCN)	ENSP00000285071.4:p.Ser575_Ser577delinsProGlnPro
ENST00000427497.3:c.*372+1313_*372+1319delinsCCACAGC	ENSP00000394249.3:n.*372+1313_*372+1319delinsCCACAGC
ENST00000578209.5:c.562-3824_562-3818delinsGCTGTGG (MPRIP)
NM_144997.5:c.1723_1729delinsCCACAGC , LRG_325t1:c.1723_1729delinsCCACAGC (FLCN)	NP_659434.2:p.Ser575_Ser577delinsProGlnPro
XM_011523714.1:c.1777_1783delinsCCACAGC (FLCN)	XP_011522016.1:p.Ser593_Ser595delinsProGlnPro
XM_011523715.1:c.1777_1783delinsCCACAGC (FLCN)	XP_011522017.1:p.Ser593_Ser595delinsProGlnPro
XM_011523716.1:c.1777_1783delinsCCACAGC (FLCN)	XP_011522018.1:p.Ser593_Ser595delinsProGlnPro
XM_011523717.1:c.1777_1783delinsCCACAGC (FLCN)	XP_011522019.1:p.Ser593_Ser595delinsProGlnPro
XM_011523718.1:c.1777_1783delinsCCACAGC (FLCN)	XP_011522020.1:p.Ser593_Ser595delinsProGlnPro
XM_011523719.1:c.1592+1313_1592+1319delinsCCACAGC (FLCN)	XP_011522021.1:n.1592+1313_1592+1319delinsCCACAGC
XM_011523720.1:c.1501_1507delinsCCACAGC (FLCN)	XP_011522022.1:p.Ser501_Ser503delinsProGlnPro
XM_011523721.1:c.1777_1783delinsCCACAGC (FLCN)	XP_011522023.1:p.Ser593_Ser595delinsProGlnPro
NM_001353229.1:c.1777_1783delinsCCACAGC (FLCN)	NP_001340158.1:p.Ser593_Ser595delinsProGlnPro
NM_001353230.1:c.1723_1729delinsCCACAGC (FLCN)	NP_001340159.1:p.Ser575_Ser577delinsProGlnPro
NM_001353231.1:c.1723_1729delinsCCACAGC (FLCN)	NP_001340160.1:p.Ser575_Ser577delinsProGlnPro
NM_144997.6:c.1723_1729delinsCCACAGC (FLCN)	NP_659434.2:p.Ser575_Ser577delinsProGlnPro
XM_011523714.3:c.1777_1783delinsCCACAGC (FLCN)	XP_011522016.1:p.Ser593_Ser595delinsProGlnPro
XM_011523718.3:c.1777_1783delinsCCACAGC (FLCN)	XP_011522020.1:p.Ser593_Ser595delinsProGlnPro
XM_011523719.3:c.1592+1313_1592+1319delinsCCACAGC (FLCN)	XP_011522021.1:n.1592+1313_1592+1319delinsCCACAGC
XM_011523721.3:c.1777_1783delinsCCACAGC (FLCN)	XP_011522023.1:p.Ser593_Ser595delinsProGlnPro
XM_017024305.2:c.1777_1783delinsCCACAGC (FLCN)	XP_016879794.1:p.Ser593_Ser595delinsProGlnPro
XM_017024308.1:c.1723_1729delinsCCACAGC (FLCN)	XP_016879797.1:p.Ser575_Ser577delinsProGlnPro
XM_017024309.2:c.1501_1507delinsCCACAGC (FLCN)	XP_016879798.1:p.Ser501_Ser503delinsProGlnPro
XM_024450635.1:c.1777_1783delinsCCACAGC (FLCN)	XP_024306403.1:p.Ser593_Ser595delinsProGlnPro
XR_001752445.2:n.2157_2163delinsCCACAGC (FLCN)
NM_144997.7:c.1723_1729delinsCCACAGC (FLCN) MANE Select	NP_659434.2:p.Ser575_Ser577delinsProGlnPro
NM_001353229.2:c.1777_1783delinsCCACAGC (FLCN)	NP_001340158.1:p.Ser593_Ser595delinsProGlnPro
NM_001353230.2:c.1723_1729delinsCCACAGC (FLCN)	NP_001340159.1:p.Ser575_Ser577delinsProGlnPro
NM_001353231.2:c.1723_1729delinsCCACAGC (FLCN)	NP_001340160.1:p.Ser575_Ser577delinsProGlnPro