Canonical Allele Identifier: CA2250418910

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17218930G= , CM000679.2:g.17218930G=	GRCh38
NC_000017.10:g.17122244G= , CM000679.1:g.17122244G=	GRCh37
NC_000017.9:g.17062969G=	NCBI36
NG_008001.2:g.23259C= , LRG_325:g.23259C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.1062+89C= MANE Select	ENSP00000285071.4:n.1062+89C=
ENST00000285071.8:c.1062+89C=	ENSP00000285071.4:n.1062+89C=
ENST00000427497.3:c.184+89C=	ENSP00000394249.3:n.184+89C=
ENST00000577591.1:n.85+89C=
NM_144997.5:c.1062+89C= , LRG_325t1:c.1062+89C=	NP_659434.2:n.1062+89C=
XM_011523714.1:c.1116+89C=	XP_011522016.1:n.1116+89C=
XM_011523715.1:c.1116+89C=	XP_011522017.1:n.1116+89C=
XM_011523716.1:c.1116+89C=	XP_011522018.1:n.1116+89C=
XM_011523717.1:c.1116+89C=	XP_011522019.1:n.1116+89C=
XM_011523718.1:c.1116+89C=	XP_011522020.1:n.1116+89C=
XM_011523719.1:c.1116+89C=	XP_011522021.1:n.1116+89C=
XM_011523720.1:c.840+89C=	XP_011522022.1:n.840+89C=
XM_011523721.1:c.1116+89C=	XP_011522023.1:n.1116+89C=
XR_934007.1:n.2456+89C=
NM_001353229.1:c.1116+89C=	NP_001340158.1:n.1116+89C=
NM_001353230.1:c.1062+89C=	NP_001340159.1:n.1062+89C=
NM_001353231.1:c.1062+89C=	NP_001340160.1:n.1062+89C=
NM_144997.6:c.1062+89C=	NP_659434.2:n.1062+89C=
XM_011523714.3:c.1116+89C=	XP_011522016.1:n.1116+89C=
XM_011523718.3:c.1116+89C=	XP_011522020.1:n.1116+89C=
XM_011523719.3:c.1116+89C=	XP_011522021.1:n.1116+89C=
XM_011523721.3:c.1116+89C=	XP_011522023.1:n.1116+89C=
XM_017024305.2:c.1116+89C=	XP_016879794.1:n.1116+89C=
XM_017024308.1:c.1062+89C=	XP_016879797.1:n.1062+89C=
XM_017024309.2:c.840+89C=	XP_016879798.1:n.840+89C=
XM_024450635.1:c.1116+89C=	XP_024306403.1:n.1116+89C=
XR_001752445.2:n.1620+89C=
NM_144997.7:c.1062+89C= MANE Select	NP_659434.2:n.1062+89C=
NM_001353229.2:c.1116+89C=	NP_001340158.1:n.1116+89C=
NM_001353230.2:c.1062+89C=	NP_001340159.1:n.1062+89C=
NM_001353231.2:c.1062+89C=	NP_001340160.1:n.1062+89C=