Canonical Allele Identifier: CA2250418174

Gene: FLCN MPRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217233_17217240delinsCTCTCCCT , CM000679.2:g.17217233_17217240delinsCTCTCCCT	GRCh38
NC_000017.10:g.17120547_17120554delinsCTCTCCCT , CM000679.1:g.17120547_17120554delinsCTCTCCCT	GRCh37
NC_000017.9:g.17061272_17061279delinsCTCTCCCT	NCBI36
NG_008001.2:g.24949_24956delinsAGGGAGAG , LRG_325:g.24949_24956delinsAGGGAGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.1063-58_1063-51delinsAGGGAGAG (FLCN) MANE Select	ENSP00000285071.4:n.1063-58_1063-51delinsAGGGAGAG
ENST00000285071.8:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	ENSP00000285071.4:n.1063-58_1063-51delinsAGGGAGAG
ENST00000427497.3:c.185-58_185-51delinsAGGGAGAG	ENSP00000394249.3:n.185-58_185-51delinsAGGGAGAG
ENST00000577591.1:n.86-58_86-51delinsAGGGAGAG (FLCN)
ENST00000578209.5:c.562-257_562-250delinsCTCTCCCT (MPRIP)
NM_144997.5:c.1063-58_1063-51delinsAGGGAGAG , LRG_325t1:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	NP_659434.2:n.1063-58_1063-51delinsAGGGAGAG
XM_011523714.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522016.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523715.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522017.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523716.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522018.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523717.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522019.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523718.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522020.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523719.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522021.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523720.1:c.841-58_841-51delinsAGGGAGAG (FLCN)	XP_011522022.1:n.841-58_841-51delinsAGGGAGAG
XM_011523721.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522023.1:n.1117-58_1117-51delinsAGGGAGAG
XR_934007.1:n.2457-58_2457-51delinsAGGGAGAG (FLCN)
NM_001353229.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	NP_001340158.1:n.1117-58_1117-51delinsAGGGAGAG
NM_001353230.1:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	NP_001340159.1:n.1063-58_1063-51delinsAGGGAGAG
NM_001353231.1:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	NP_001340160.1:n.1063-58_1063-51delinsAGGGAGAG
NM_144997.6:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	NP_659434.2:n.1063-58_1063-51delinsAGGGAGAG
XM_011523714.3:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522016.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523718.3:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522020.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523719.3:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522021.1:n.1117-58_1117-51delinsAGGGAGAG
XM_011523721.3:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_011522023.1:n.1117-58_1117-51delinsAGGGAGAG
XM_017024305.2:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_016879794.1:n.1117-58_1117-51delinsAGGGAGAG
XM_017024308.1:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	XP_016879797.1:n.1063-58_1063-51delinsAGGGAGAG
XM_017024309.2:c.841-58_841-51delinsAGGGAGAG (FLCN)	XP_016879798.1:n.841-58_841-51delinsAGGGAGAG
XM_024450635.1:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	XP_024306403.1:n.1117-58_1117-51delinsAGGGAGAG
XR_001752445.2:n.1621-58_1621-51delinsAGGGAGAG (FLCN)
NM_144997.7:c.1063-58_1063-51delinsAGGGAGAG (FLCN) MANE Select	NP_659434.2:n.1063-58_1063-51delinsAGGGAGAG
NM_001353229.2:c.1117-58_1117-51delinsAGGGAGAG (FLCN)	NP_001340158.1:n.1117-58_1117-51delinsAGGGAGAG
NM_001353230.2:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	NP_001340159.1:n.1063-58_1063-51delinsAGGGAGAG
NM_001353231.2:c.1063-58_1063-51delinsAGGGAGAG (FLCN)	NP_001340160.1:n.1063-58_1063-51delinsAGGGAGAG