Canonical Allele Identifier: CA10648714

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17236983G>A , CM000679.2:g.17236983G>A	GRCh38
NC_000017.10:g.17140297G>A , CM000679.1:g.17140297G>A	GRCh37
NC_000017.9:g.17081022G>A	NCBI36
NG_008001.2:g.5206C>T , LRG_325:g.5206C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_144997.7:c.-299C>T MANE Select	NP_659434.2:n.-299C>T
ENST00000285071.9:c.-299C>T MANE Select	ENSP00000285071.4:n.-299C>T
NM_001353229.1:c.-507C>T	NP_001340158.1:n.-507C>T
NM_001353229.2:c.-507C>T	NP_001340158.1:n.-507C>T
NM_001353230.1:c.-582C>T	NP_001340159.1:n.-582C>T
NM_001353230.2:c.-582C>T	NP_001340159.1:n.-582C>T
NM_001353231.1:c.-498C>T	NP_001340160.1:n.-498C>T
NM_001353231.2:c.-498C>T	NP_001340160.1:n.-498C>T
NM_144606.5:c.-299C>T	NP_653207.1:n.-299C>T
NM_144606.6:c.-299C>T	NP_653207.1:n.-299C>T
NM_144606.7:c.-299C>T	NP_653207.1:n.-299C>T
NM_144997.5:c.-299C>T , LRG_325t1:c.-299C>T	NP_659434.2:n.-299C>T
NM_144997.6:c.-299C>T	NP_659434.2:n.-299C>T
ENST00000285071.8:c.-299C>T	ENSP00000285071.4:n.-299C>T
ENST00000389169.9:c.-299C>T	ENSP00000373821.5:n.-299C>T
ENST00000389171.4:n.206C>T
ENST00000417064.1:c.-99C>T	ENSP00000410410.1:n.-99C>T
ENST00000427497.3:c.-299C>T	ENSP00000394249.3:n.-299C>T
XM_011523714.1:c.-299C>T	XP_011522016.1:n.-299C>T
XM_011523714.3:c.-299C>T	XP_011522016.1:n.-299C>T
XM_011523715.1:c.-1043C>T	XP_011522017.1:n.-1043C>T
XM_011523717.1:c.-959C>T	XP_011522019.1:n.-959C>T
XM_011523718.1:c.-210C>T	XP_011522020.1:n.-210C>T
XM_011523718.3:c.-210C>T	XP_011522020.1:n.-210C>T
XM_011523719.3:c.-299C>T	XP_011522021.1:n.-299C>T
XM_017024305.2:c.-498C>T	XP_016879794.1:n.-498C>T
XM_017024308.1:c.-706C>T	XP_016879797.1:n.-706C>T
XM_017024309.2:c.-299C>T	XP_016879798.1:n.-299C>T
XM_024450635.1:c.-1507C>T	XP_024306403.1:n.-1507C>T
XR_001752445.2:n.206C>T