Canonical Allele Identifier: CA915949600

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17219128_17219129insTCTGTACTCTCTGGCAACACAGGGGCTT , CM000679.2:g.17219128_17219129insTCTGTACTCTCTGGCAACACAGGGGCTT	GRCh38
NC_000017.10:g.17122442_17122443insTCTGTACTCTCTGGCAACACAGGGGCTT , CM000679.1:g.17122442_17122443insTCTGTACTCTCTGGCAACACAGGGGCTT	GRCh37
NC_000017.9:g.17063167_17063168insTCTGTACTCTCTGGCAACACAGGGGCTT	NCBI36
NG_008001.2:g.23063_23064insCCCCTGTGTTGCCAGAGAGTACAGAAAG , LRG_325:g.23063_23064insCCCCTGTGTTGCCAGAGAGTACAGAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG MANE Select	ENSP00000285071.4:p.Gly319AlafsTer?
ENST00000285071.8:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	ENSP00000285071.4:p.Gly319AlafsTer?
ENST00000427497.3:c.149-72_149-71insCCCCTGTGTTGCCAGAGAGTACAGAAAG	ENSP00000394249.3:n.149-72_149-71insCCCCTGTGTTGCCAGAGAGTACAGA...
NM_144997.5:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG , LRG_325t1:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_659434.2:p.Gly319AlafsTer?
XM_011523714.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522016.1:p.Gly337AlafsTer?
XM_011523715.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522017.1:p.Gly337AlafsTer?
XM_011523716.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522018.1:p.Gly337AlafsTer?
XM_011523717.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522019.1:p.Gly337AlafsTer?
XM_011523718.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522020.1:p.Gly337AlafsTer?
XM_011523719.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522021.1:p.Gly337AlafsTer?
XM_011523720.1:c.733_734insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522022.1:p.Gly245AlafsTer?
XM_011523721.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522023.1:p.Gly337AlafsTer?
XR_934007.1:n.2349_2350insCCCCTGTGTTGCCAGAGAGTACAGAAAG
NM_001353229.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_001340158.1:p.Gly337AlafsTer?
NM_001353230.1:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_001340159.1:p.Gly319AlafsTer?
NM_001353231.1:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_001340160.1:p.Gly319AlafsTer?
NM_144997.6:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_659434.2:p.Gly319AlafsTer?
XM_011523714.3:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522016.1:p.Gly337AlafsTer?
XM_011523718.3:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522020.1:p.Gly337AlafsTer?
XM_011523719.3:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522021.1:p.Gly337AlafsTer?
XM_011523721.3:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_011522023.1:p.Gly337AlafsTer?
XM_017024305.2:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_016879794.1:p.Gly337AlafsTer?
XM_017024308.1:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_016879797.1:p.Gly319AlafsTer?
XM_017024309.2:c.733_734insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_016879798.1:p.Gly245AlafsTer?
XM_024450635.1:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	XP_024306403.1:p.Gly337AlafsTer?
XR_001752445.2:n.1513_1514insCCCCTGTGTTGCCAGAGAGTACAGAAAG
NM_144997.7:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG MANE Select	NP_659434.2:p.Gly319AlafsTer?
NM_001353229.2:c.1009_1010insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_001340158.1:p.Gly337AlafsTer?
NM_001353230.2:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_001340159.1:p.Gly319AlafsTer?
NM_001353231.2:c.955_956insCCCCTGTGTTGCCAGAGAGTACAGAAAG	NP_001340160.1:p.Gly319AlafsTer?