Canonical Allele Identifier: CA2250421054

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17228460_17228461delinsTC , CM000679.2:g.17228460_17228461delinsTC	GRCh38
NC_000017.10:g.17131774_17131775delinsTC , CM000679.1:g.17131774_17131775delinsTC	GRCh37
NC_000017.9:g.17072499_17072500delinsTC	NCBI36
NG_008001.2:g.13728_13729delinsGA , LRG_325:g.13728_13729delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.-24-300_-24-299delinsGA MANE Select	ENSP00000285071.4:n.-24-300_-24-299delinsGA
ENST00000285071.8:c.-24-300_-24-299delinsGA	ENSP00000285071.4:n.-24-300_-24-299delinsGA
ENST00000389168.6:n.1017_1018delinsGA
ENST00000389169.9:c.-24-300_-24-299delinsGA	ENSP00000373821.5:n.-24-300_-24-299delinsGA
ENST00000389171.4:n.481-300_481-299delinsGA
ENST00000417064.1:c.-27-456_-27-455delinsGA	ENSP00000410410.1:n.-27-456_-27-455delinsGA
ENST00000427497.3:c.-24-300_-24-299delinsGA	ENSP00000394249.3:n.-24-300_-24-299delinsGA
ENST00000461699.1:c.-25+162_-25+163delinsGA	ENSP00000463970.1:n.-25+162_-25+163delinsGA
NM_144606.5:c.-24-300_-24-299delinsGA	NP_653207.1:n.-24-300_-24-299delinsGA
NM_144997.5:c.-24-300_-24-299delinsGA , LRG_325t1:c.-24-300_-24-299delinsGA	NP_659434.2:n.-24-300_-24-299delinsGA
XM_011523714.1:c.-24-300_-24-299delinsGA	XP_011522016.1:n.-24-300_-24-299delinsGA
XM_011523715.1:c.-324_-323delinsGA	XP_011522017.1:n.-324_-323delinsGA
XM_011523716.1:c.-25+162_-25+163delinsGA	XP_011522018.1:n.-25+162_-25+163delinsGA
XM_011523717.1:c.-324_-323delinsGA	XP_011522019.1:n.-324_-323delinsGA
XM_011523718.1:c.-24-300_-24-299delinsGA	XP_011522020.1:n.-24-300_-24-299delinsGA
XM_011523719.1:c.-324_-323delinsGA	XP_011522021.1:n.-324_-323delinsGA
XM_011523720.1:c.-324_-323delinsGA	XP_011522022.1:n.-324_-323delinsGA
XM_011523721.1:c.-24-300_-24-299delinsGA	XP_011522023.1:n.-24-300_-24-299delinsGA
XR_934007.1:n.1017_1018delinsGA
NM_001353229.1:c.-24-300_-24-299delinsGA	NP_001340158.1:n.-24-300_-24-299delinsGA
NM_001353230.1:c.-25+162_-25+163delinsGA	NP_001340159.1:n.-25+162_-25+163delinsGA
NM_001353231.1:c.-25+162_-25+163delinsGA	NP_001340160.1:n.-25+162_-25+163delinsGA
NM_144606.6:c.-24-300_-24-299delinsGA	NP_653207.1:n.-24-300_-24-299delinsGA
NM_144997.6:c.-24-300_-24-299delinsGA	NP_659434.2:n.-24-300_-24-299delinsGA
XM_011523714.3:c.-24-300_-24-299delinsGA	XP_011522016.1:n.-24-300_-24-299delinsGA
XM_011523718.3:c.-24-300_-24-299delinsGA	XP_011522020.1:n.-24-300_-24-299delinsGA
XM_011523719.3:c.-24-300_-24-299delinsGA	XP_011522021.1:n.-24-300_-24-299delinsGA
XM_011523721.3:c.-24-300_-24-299delinsGA	XP_011522023.1:n.-24-300_-24-299delinsGA
XM_017024305.2:c.-25+162_-25+163delinsGA	XP_016879794.1:n.-25+162_-25+163delinsGA
XM_017024308.1:c.-25+162_-25+163delinsGA	XP_016879797.1:n.-25+162_-25+163delinsGA
XM_017024309.2:c.-24-300_-24-299delinsGA	XP_016879798.1:n.-24-300_-24-299delinsGA
XM_024450635.1:c.-25+162_-25+163delinsGA	XP_024306403.1:n.-25+162_-25+163delinsGA
XR_001752445.2:n.481-300_481-299delinsGA
NM_144997.7:c.-24-300_-24-299delinsGA MANE Select	NP_659434.2:n.-24-300_-24-299delinsGA
NM_001353229.2:c.-24-300_-24-299delinsGA	NP_001340158.1:n.-24-300_-24-299delinsGA
NM_001353230.2:c.-25+162_-25+163delinsGA	NP_001340159.1:n.-25+162_-25+163delinsGA
NM_001353231.2:c.-25+162_-25+163delinsGA	NP_001340160.1:n.-25+162_-25+163delinsGA
NM_144606.7:c.-24-300_-24-299delinsGA	NP_653207.1:n.-24-300_-24-299delinsGA