Canonical Allele Identifier: CA2250417690

Gene: FLCN MPRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17216625_17216628delinsAGAG , CM000679.2:g.17216625_17216628delinsAGAG	GRCh38
NC_000017.10:g.17119939_17119942delinsAGAG , CM000679.1:g.17119939_17119942delinsAGAG	GRCh37
NC_000017.9:g.17060664_17060667delinsAGAG	NCBI36
NG_008001.2:g.25561_25564delinsCTCT , LRG_325:g.25561_25564delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1177-125_1177-122delinsCTCT (FLCN) MANE Select	ENSP00000285071.4:n.1177-125_1177-122delinsCTCT
ENST00000285071.8:c.1177-125_1177-122delinsCTCT (FLCN)	ENSP00000285071.4:n.1177-125_1177-122delinsCTCT
ENST00000427497.3:c.*11-125_*11-122delinsCTCT	ENSP00000394249.3:n.*11-125_*11-122delinsCTCT
ENST00000578209.5:c.562-865_562-862delinsAGAG (MPRIP)
NM_144997.5:c.1177-125_1177-122delinsCTCT , LRG_325t1:c.1177-125_1177-122delinsCTCT (FLCN)	NP_659434.2:n.1177-125_1177-122delinsCTCT
XM_011523714.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522016.1:n.1231-125_1231-122delinsCTCT
XM_011523715.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522017.1:n.1231-125_1231-122delinsCTCT
XM_011523716.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522018.1:n.1231-125_1231-122delinsCTCT
XM_011523717.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522019.1:n.1231-125_1231-122delinsCTCT
XM_011523718.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522020.1:n.1231-125_1231-122delinsCTCT
XM_011523719.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522021.1:n.1231-125_1231-122delinsCTCT
XM_011523720.1:c.955-125_955-122delinsCTCT (FLCN)	XP_011522022.1:n.955-125_955-122delinsCTCT
XM_011523721.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522023.1:n.1231-125_1231-122delinsCTCT
XR_934007.1:n.2570+441_2570+444delinsCTCT (FLCN)
NM_001353229.1:c.1231-125_1231-122delinsCTCT (FLCN)	NP_001340158.1:n.1231-125_1231-122delinsCTCT
NM_001353230.1:c.1177-125_1177-122delinsCTCT (FLCN)	NP_001340159.1:n.1177-125_1177-122delinsCTCT
NM_001353231.1:c.1177-125_1177-122delinsCTCT (FLCN)	NP_001340160.1:n.1177-125_1177-122delinsCTCT
NM_144997.6:c.1177-125_1177-122delinsCTCT (FLCN)	NP_659434.2:n.1177-125_1177-122delinsCTCT
XM_011523714.3:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522016.1:n.1231-125_1231-122delinsCTCT
XM_011523718.3:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522020.1:n.1231-125_1231-122delinsCTCT
XM_011523719.3:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522021.1:n.1231-125_1231-122delinsCTCT
XM_011523721.3:c.1231-125_1231-122delinsCTCT (FLCN)	XP_011522023.1:n.1231-125_1231-122delinsCTCT
XM_017024305.2:c.1231-125_1231-122delinsCTCT (FLCN)	XP_016879794.1:n.1231-125_1231-122delinsCTCT
XM_017024308.1:c.1177-125_1177-122delinsCTCT (FLCN)	XP_016879797.1:n.1177-125_1177-122delinsCTCT
XM_017024309.2:c.955-125_955-122delinsCTCT (FLCN)	XP_016879798.1:n.955-125_955-122delinsCTCT
XM_024450635.1:c.1231-125_1231-122delinsCTCT (FLCN)	XP_024306403.1:n.1231-125_1231-122delinsCTCT
XR_001752445.2:n.1734+441_1734+444delinsCTCT (FLCN)
NM_144997.7:c.1177-125_1177-122delinsCTCT (FLCN) MANE Select	NP_659434.2:n.1177-125_1177-122delinsCTCT
NM_001353229.2:c.1231-125_1231-122delinsCTCT (FLCN)	NP_001340158.1:n.1231-125_1231-122delinsCTCT
NM_001353230.2:c.1177-125_1177-122delinsCTCT (FLCN)	NP_001340159.1:n.1177-125_1177-122delinsCTCT
NM_001353231.2:c.1177-125_1177-122delinsCTCT (FLCN)	NP_001340160.1:n.1177-125_1177-122delinsCTCT