Canonical Allele Identifier: CA2250419062

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17219209T= , CM000679.2:g.17219209T=	GRCh38
NC_000017.10:g.17122523T= , CM000679.1:g.17122523T=	GRCh37
NC_000017.9:g.17063248T=	NCBI36
NG_008001.2:g.22980A= , LRG_325:g.22980A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.872A= MANE Select	ENSP00000285071.4:p.Asp291=
ENST00000285071.8:c.872A=	ENSP00000285071.4:p.Asp291=
ENST00000427497.3:c.149-155A=	ENSP00000394249.3:n.149-155A=
NM_144997.5:c.872A= , LRG_325t1:c.872A=	NP_659434.2:p.Asp291=
XM_011523714.1:c.926A=	XP_011522016.1:p.Asp309=
XM_011523715.1:c.926A=	XP_011522017.1:p.Asp309=
XM_011523716.1:c.926A=	XP_011522018.1:p.Asp309=
XM_011523717.1:c.926A=	XP_011522019.1:p.Asp309=
XM_011523718.1:c.926A=	XP_011522020.1:p.Asp309=
XM_011523719.1:c.926A=	XP_011522021.1:p.Asp309=
XM_011523720.1:c.650A=	XP_011522022.1:p.Asp217=
XM_011523721.1:c.926A=	XP_011522023.1:p.Asp309=
XR_934007.1:n.2266A=
NM_001353229.1:c.926A=	NP_001340158.1:p.Asp309=
NM_001353230.1:c.872A=	NP_001340159.1:p.Asp291=
NM_001353231.1:c.872A=	NP_001340160.1:p.Asp291=
NM_144997.6:c.872A=	NP_659434.2:p.Asp291=
XM_011523714.3:c.926A=	XP_011522016.1:p.Asp309=
XM_011523718.3:c.926A=	XP_011522020.1:p.Asp309=
XM_011523719.3:c.926A=	XP_011522021.1:p.Asp309=
XM_011523721.3:c.926A=	XP_011522023.1:p.Asp309=
XM_017024305.2:c.926A=	XP_016879794.1:p.Asp309=
XM_017024308.1:c.872A=	XP_016879797.1:p.Asp291=
XM_017024309.2:c.650A=	XP_016879798.1:p.Asp217=
XM_024450635.1:c.926A=	XP_024306403.1:p.Asp309=
XR_001752445.2:n.1430A=
NM_144997.7:c.872A= MANE Select	NP_659434.2:p.Asp291=
NM_001353229.2:c.926A=	NP_001340158.1:p.Asp309=
NM_001353230.2:c.872A=	NP_001340159.1:p.Asp291=
NM_001353231.2:c.872A=	NP_001340160.1:p.Asp291=