Canonical Allele Identifier: CA3260671893

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17221527_17222671del , CM000679.2:g.17221527_17222671del	GRCh38
NC_000017.10:g.17124841_17125985del , CM000679.1:g.17124841_17125985del	GRCh37
NC_000017.9:g.17065566_17066710del	NCBI36
NG_008001.2:g.19518_20662del , LRG_325:g.19518_20662del

Transcript Alleles

HGVS	Amino-acid Change
NM_001353229.1:c.673-10_925+10del
NM_001353229.2:c.673-10_925+10del
NM_001353230.1:c.619-10_871+10del
NM_001353230.2:c.619-10_871+10del
NM_001353231.1:c.619-10_871+10del
NM_001353231.2:c.619-10_871+10del
NM_144606.5:c.619-10_881del
NM_144606.6:c.619-10_881del
NM_144606.7:c.619-10_881del
NM_144997.5:c.619-10_871+10del , LRG_325t1:c.619-10_871+10del
NM_144997.6:c.619-10_871+10del
NM_144997.7:c.619-10_871+10del
ENST00000285071.8:c.619-10_871+10del
ENST00000285071.9:c.619-10_871+10del
ENST00000389169.9:c.619-10_881del
ENST00000427497.3:c.149-3617_149-2473del	ENSP00000394249.3:n.149-3617_149-2473del
ENST00000466317.1:n.452_724del
XM_011523714.1:c.673-10_925+10del
XM_011523714.3:c.673-10_925+10del
XM_011523715.1:c.673-10_925+10del
XM_011523716.1:c.673-10_925+10del
XM_011523717.1:c.673-10_925+10del
XM_011523718.1:c.673-10_925+10del
XM_011523718.3:c.673-10_925+10del
XM_011523719.1:c.673-10_925+10del
XM_011523719.3:c.673-10_925+10del
XM_011523720.1:c.397-10_649+10del
XM_011523721.1:c.673-10_925+10del
XM_011523721.3:c.673-10_925+10del
XM_017024305.2:c.673-10_925+10del
XM_017024308.1:c.619-10_871+10del
XM_017024309.2:c.397-10_649+10del
XM_024450635.1:c.673-10_925+10del
XR_001752445.2:n.1177-10_1429+10del
XR_934007.1:n.2013-10_2265+10del