Canonical Allele Identifier: CA2636358026

Gene: FLCN

Linked Data

• gnomAD v4: 17-17227962-C-CTGGAGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17227962_17227963insTGGAGCT , CM000679.2:g.17227962_17227963insTGGAGCT	GRCh38
NC_000017.10:g.17131276_17131277insTGGAGCT , CM000679.1:g.17131276_17131277insTGGAGCT	GRCh37
NC_000017.9:g.17072001_17072002insTGGAGCT	NCBI36
NG_008001.2:g.14226_14227insAGCTCCA , LRG_325:g.14226_14227insAGCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.175_176insAGCTCCA MANE Select	ENSP00000285071.4:p.Arg59GlnfsTer?
ENST00000285071.8:c.175_176insAGCTCCA	ENSP00000285071.4:p.Arg59GlnfsTer?
ENST00000389168.6:n.1515_1516insAGCTCCA
ENST00000389169.9:c.175_176insAGCTCCA	ENSP00000373821.5:p.Arg59GlnfsTer?
ENST00000389171.4:n.679_680insAGCTCCA
ENST00000417064.1:c.16_17insAGCTCCA	ENSP00000410410.1:p.Arg6GlnfsTer?
ENST00000427497.3:c.148+27_148+28insAGCTCCA	ENSP00000394249.3:n.148+27_148+28insAGCTCCA
NM_144606.5:c.175_176insAGCTCCA	NP_653207.1:p.Arg59GlnfsTer?
NM_144997.5:c.175_176insAGCTCCA , LRG_325t1:c.175_176insAGCTCCA	NP_659434.2:p.Arg59GlnfsTer?
XM_011523714.1:c.175_176insAGCTCCA	XP_011522016.1:p.Arg59GlnfsTer?
XM_011523715.1:c.175_176insAGCTCCA	XP_011522017.1:p.Arg59GlnfsTer?
XM_011523716.1:c.175_176insAGCTCCA	XP_011522018.1:p.Arg59GlnfsTer?
XM_011523717.1:c.175_176insAGCTCCA	XP_011522019.1:p.Arg59GlnfsTer?
XM_011523718.1:c.175_176insAGCTCCA	XP_011522020.1:p.Arg59GlnfsTer?
XM_011523719.1:c.175_176insAGCTCCA	XP_011522021.1:p.Arg59GlnfsTer?
XM_011523720.1:c.175_176insAGCTCCA	XP_011522022.1:p.Arg59GlnfsTer?
XM_011523721.1:c.175_176insAGCTCCA	XP_011522023.1:p.Arg59GlnfsTer?
XR_934007.1:n.1515_1516insAGCTCCA
NM_001353229.1:c.175_176insAGCTCCA	NP_001340158.1:p.Arg59GlnfsTer?
NM_001353230.1:c.175_176insAGCTCCA	NP_001340159.1:p.Arg59GlnfsTer?
NM_001353231.1:c.175_176insAGCTCCA	NP_001340160.1:p.Arg59GlnfsTer?
NM_144606.6:c.175_176insAGCTCCA	NP_653207.1:p.Arg59GlnfsTer?
NM_144997.6:c.175_176insAGCTCCA	NP_659434.2:p.Arg59GlnfsTer?
XM_011523714.3:c.175_176insAGCTCCA	XP_011522016.1:p.Arg59GlnfsTer?
XM_011523718.3:c.175_176insAGCTCCA	XP_011522020.1:p.Arg59GlnfsTer?
XM_011523719.3:c.175_176insAGCTCCA	XP_011522021.1:p.Arg59GlnfsTer?
XM_011523721.3:c.175_176insAGCTCCA	XP_011522023.1:p.Arg59GlnfsTer?
XM_017024305.2:c.175_176insAGCTCCA	XP_016879794.1:p.Arg59GlnfsTer?
XM_017024308.1:c.175_176insAGCTCCA	XP_016879797.1:p.Arg59GlnfsTer?
XM_017024309.2:c.175_176insAGCTCCA	XP_016879798.1:p.Arg59GlnfsTer?
XM_024450635.1:c.175_176insAGCTCCA	XP_024306403.1:p.Arg59GlnfsTer?
XR_001752445.2:n.679_680insAGCTCCA
NM_144997.7:c.175_176insAGCTCCA MANE Select	NP_659434.2:p.Arg59GlnfsTer?
NM_001353229.2:c.175_176insAGCTCCA	NP_001340158.1:p.Arg59GlnfsTer?
NM_001353230.2:c.175_176insAGCTCCA	NP_001340159.1:p.Arg59GlnfsTer?
NM_001353231.2:c.175_176insAGCTCCA	NP_001340160.1:p.Arg59GlnfsTer?
NM_144606.7:c.175_176insAGCTCCA	NP_653207.1:p.Arg59GlnfsTer?