Canonical Allele Identifier: CA2840315831

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17218924A>C , CM000679.2:g.17218924A>C	GRCh38
NC_000017.10:g.17122238A>C , CM000679.1:g.17122238A>C	GRCh37
NC_000017.9:g.17062963A>C	NCBI36
NG_008001.2:g.23265T>G , LRG_325:g.23265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1062+95T>G MANE Select	ENSP00000285071.4:n.1062+95T>G
ENST00000285071.8:c.1062+95T>G	ENSP00000285071.4:n.1062+95T>G
ENST00000427497.3:c.184+95T>G	ENSP00000394249.3:n.184+95T>G
ENST00000577591.1:n.85+95T>G
NM_144997.5:c.1062+95T>G , LRG_325t1:c.1062+95T>G	NP_659434.2:n.1062+95T>G
XM_011523714.1:c.1116+95T>G	XP_011522016.1:n.1116+95T>G
XM_011523715.1:c.1116+95T>G	XP_011522017.1:n.1116+95T>G
XM_011523716.1:c.1116+95T>G	XP_011522018.1:n.1116+95T>G
XM_011523717.1:c.1116+95T>G	XP_011522019.1:n.1116+95T>G
XM_011523718.1:c.1116+95T>G	XP_011522020.1:n.1116+95T>G
XM_011523719.1:c.1116+95T>G	XP_011522021.1:n.1116+95T>G
XM_011523720.1:c.840+95T>G	XP_011522022.1:n.840+95T>G
XM_011523721.1:c.1116+95T>G	XP_011522023.1:n.1116+95T>G
XR_934007.1:n.2456+95T>G
NM_001353229.1:c.1116+95T>G	NP_001340158.1:n.1116+95T>G
NM_001353230.1:c.1062+95T>G	NP_001340159.1:n.1062+95T>G
NM_001353231.1:c.1062+95T>G	NP_001340160.1:n.1062+95T>G
NM_144997.6:c.1062+95T>G	NP_659434.2:n.1062+95T>G
XM_011523714.3:c.1116+95T>G	XP_011522016.1:n.1116+95T>G
XM_011523718.3:c.1116+95T>G	XP_011522020.1:n.1116+95T>G
XM_011523719.3:c.1116+95T>G	XP_011522021.1:n.1116+95T>G
XM_011523721.3:c.1116+95T>G	XP_011522023.1:n.1116+95T>G
XM_017024305.2:c.1116+95T>G	XP_016879794.1:n.1116+95T>G
XM_017024308.1:c.1062+95T>G	XP_016879797.1:n.1062+95T>G
XM_017024309.2:c.840+95T>G	XP_016879798.1:n.840+95T>G
XM_024450635.1:c.1116+95T>G	XP_024306403.1:n.1116+95T>G
XR_001752445.2:n.1620+95T>G
NM_144997.7:c.1062+95T>G MANE Select	NP_659434.2:n.1062+95T>G
NM_001353229.2:c.1116+95T>G	NP_001340158.1:n.1116+95T>G
NM_001353230.2:c.1062+95T>G	NP_001340159.1:n.1062+95T>G
NM_001353231.2:c.1062+95T>G	NP_001340160.1:n.1062+95T>G