Canonical Allele Identifier: CA2250418151

Gene: FLCN MPRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217189_17217191delinsAAG , CM000679.2:g.17217189_17217191delinsAAG	GRCh38
NC_000017.10:g.17120503_17120505delinsAAG , CM000679.1:g.17120503_17120505delinsAAG	GRCh37
NC_000017.9:g.17061228_17061230delinsAAG	NCBI36
NG_008001.2:g.24998_25000delinsCTT , LRG_325:g.24998_25000delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1063-9_1063-7delinsCTT (FLCN) MANE Select	ENSP00000285071.4:n.1063-9_1063-7delinsCTT
ENST00000285071.8:c.1063-9_1063-7delinsCTT (FLCN)	ENSP00000285071.4:n.1063-9_1063-7delinsCTT
ENST00000427497.3:c.185-9_185-7delinsCTT	ENSP00000394249.3:n.185-9_185-7delinsCTT
ENST00000577591.1:n.86-9_86-7delinsCTT (FLCN)
ENST00000578209.5:c.562-301_562-299delinsAAG (MPRIP)
NM_144997.5:c.1063-9_1063-7delinsCTT , LRG_325t1:c.1063-9_1063-7delinsCTT (FLCN)	NP_659434.2:n.1063-9_1063-7delinsCTT
XM_011523714.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522016.1:n.1117-9_1117-7delinsCTT
XM_011523715.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522017.1:n.1117-9_1117-7delinsCTT
XM_011523716.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522018.1:n.1117-9_1117-7delinsCTT
XM_011523717.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522019.1:n.1117-9_1117-7delinsCTT
XM_011523718.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522020.1:n.1117-9_1117-7delinsCTT
XM_011523719.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522021.1:n.1117-9_1117-7delinsCTT
XM_011523720.1:c.841-9_841-7delinsCTT (FLCN)	XP_011522022.1:n.841-9_841-7delinsCTT
XM_011523721.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522023.1:n.1117-9_1117-7delinsCTT
XR_934007.1:n.2457-9_2457-7delinsCTT (FLCN)
NM_001353229.1:c.1117-9_1117-7delinsCTT (FLCN)	NP_001340158.1:n.1117-9_1117-7delinsCTT
NM_001353230.1:c.1063-9_1063-7delinsCTT (FLCN)	NP_001340159.1:n.1063-9_1063-7delinsCTT
NM_001353231.1:c.1063-9_1063-7delinsCTT (FLCN)	NP_001340160.1:n.1063-9_1063-7delinsCTT
NM_144997.6:c.1063-9_1063-7delinsCTT (FLCN)	NP_659434.2:n.1063-9_1063-7delinsCTT
XM_011523714.3:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522016.1:n.1117-9_1117-7delinsCTT
XM_011523718.3:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522020.1:n.1117-9_1117-7delinsCTT
XM_011523719.3:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522021.1:n.1117-9_1117-7delinsCTT
XM_011523721.3:c.1117-9_1117-7delinsCTT (FLCN)	XP_011522023.1:n.1117-9_1117-7delinsCTT
XM_017024305.2:c.1117-9_1117-7delinsCTT (FLCN)	XP_016879794.1:n.1117-9_1117-7delinsCTT
XM_017024308.1:c.1063-9_1063-7delinsCTT (FLCN)	XP_016879797.1:n.1063-9_1063-7delinsCTT
XM_017024309.2:c.841-9_841-7delinsCTT (FLCN)	XP_016879798.1:n.841-9_841-7delinsCTT
XM_024450635.1:c.1117-9_1117-7delinsCTT (FLCN)	XP_024306403.1:n.1117-9_1117-7delinsCTT
XR_001752445.2:n.1621-9_1621-7delinsCTT (FLCN)
NM_144997.7:c.1063-9_1063-7delinsCTT (FLCN) MANE Select	NP_659434.2:n.1063-9_1063-7delinsCTT
NM_001353229.2:c.1117-9_1117-7delinsCTT (FLCN)	NP_001340158.1:n.1117-9_1117-7delinsCTT
NM_001353230.2:c.1063-9_1063-7delinsCTT (FLCN)	NP_001340159.1:n.1063-9_1063-7delinsCTT
NM_001353231.2:c.1063-9_1063-7delinsCTT (FLCN)	NP_001340160.1:n.1063-9_1063-7delinsCTT