Canonical Allele Identifier: CA2964079537

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17222501del , CM000679.2:g.17222501del	GRCh38
NC_000017.10:g.17125815del , CM000679.1:g.17125815del	GRCh37
NC_000017.9:g.17066540del	NCBI36
NG_008001.2:g.19689del , LRG_325:g.19689del

Transcript Alleles

HGVS	Amino-acid Change
NM_001353229.1:c.833+1del
NM_001353229.2:c.833+1del
NM_001353230.1:c.779+1del
NM_001353230.2:c.779+1del
NM_001353231.1:c.779+1del
NM_001353231.2:c.779+1del
NM_144606.5:c.779+1del
NM_144606.6:c.779+1del
NM_144606.7:c.779+1del
NM_144997.5:c.779+1del , LRG_325t1:c.779+1del
NM_144997.6:c.779+1del
NM_144997.7:c.779+1del
ENST00000285071.8:c.779+1del
ENST00000285071.9:c.779+1del
ENST00000389169.9:c.779+1del
ENST00000427497.3:c.149-3446del	ENSP00000394249.3:n.149-3446del
ENST00000466317.1:n.622+1del
ENST00000480316.1:n.745+1del
XM_011523714.1:c.833+1del
XM_011523714.3:c.833+1del
XM_011523715.1:c.833+1del
XM_011523716.1:c.833+1del
XM_011523717.1:c.833+1del
XM_011523718.1:c.833+1del
XM_011523718.3:c.833+1del
XM_011523719.1:c.833+1del
XM_011523719.3:c.833+1del
XM_011523720.1:c.557+1del
XM_011523721.1:c.833+1del
XM_011523721.3:c.833+1del
XM_017024305.2:c.833+1del
XM_017024308.1:c.779+1del
XM_017024309.2:c.557+1del
XM_024450635.1:c.833+1del
XR_001752445.2:n.1337+1del
XR_934007.1:n.2173+1del