Canonical Allele Identifier: CA2636354652

Gene: FLCN

Linked Data

• gnomAD v4: 17-17219287-C-CTGAAGTCACAGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17219290_17219291insAGTCACAGGATGA , CM000679.2:g.17219290_17219291insAGTCACAGGATGA	GRCh38
NC_000017.10:g.17122604_17122605insAGTCACAGGATGA , CM000679.1:g.17122604_17122605insAGTCACAGGATGA	GRCh37
NC_000017.9:g.17063329_17063330insAGTCACAGGATGA	NCBI36
NG_008001.2:g.22901_22902insTCCTGTGACTTCA , LRG_325:g.22901_22902insTCCTGTGACTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.872-79_872-78insTCCTGTGACTTCA MANE Select	ENSP00000285071.4:n.872-79_872-78insTCCTGTGACTTCA
ENST00000285071.8:c.872-79_872-78insTCCTGTGACTTCA	ENSP00000285071.4:n.872-79_872-78insTCCTGTGACTTCA
ENST00000427497.3:c.149-234_149-233insTCCTGTGACTTCA	ENSP00000394249.3:n.149-234_149-233insTCCTGTGACTTCA
NM_144997.5:c.872-79_872-78insTCCTGTGACTTCA , LRG_325t1:c.872-79_872-78insTCCTGTGACTTCA	NP_659434.2:n.872-79_872-78insTCCTGTGACTTCA
XM_011523714.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522016.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523715.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522017.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523716.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522018.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523717.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522019.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523718.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522020.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523719.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522021.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523720.1:c.650-79_650-78insTCCTGTGACTTCA	XP_011522022.1:n.650-79_650-78insTCCTGTGACTTCA
XM_011523721.1:c.926-79_926-78insTCCTGTGACTTCA	XP_011522023.1:n.926-79_926-78insTCCTGTGACTTCA
XR_934007.1:n.2266-79_2266-78insTCCTGTGACTTCA
NM_001353229.1:c.926-79_926-78insTCCTGTGACTTCA	NP_001340158.1:n.926-79_926-78insTCCTGTGACTTCA
NM_001353230.1:c.872-79_872-78insTCCTGTGACTTCA	NP_001340159.1:n.872-79_872-78insTCCTGTGACTTCA
NM_001353231.1:c.872-79_872-78insTCCTGTGACTTCA	NP_001340160.1:n.872-79_872-78insTCCTGTGACTTCA
NM_144997.6:c.872-79_872-78insTCCTGTGACTTCA	NP_659434.2:n.872-79_872-78insTCCTGTGACTTCA
XM_011523714.3:c.926-79_926-78insTCCTGTGACTTCA	XP_011522016.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523718.3:c.926-79_926-78insTCCTGTGACTTCA	XP_011522020.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523719.3:c.926-79_926-78insTCCTGTGACTTCA	XP_011522021.1:n.926-79_926-78insTCCTGTGACTTCA
XM_011523721.3:c.926-79_926-78insTCCTGTGACTTCA	XP_011522023.1:n.926-79_926-78insTCCTGTGACTTCA
XM_017024305.2:c.926-79_926-78insTCCTGTGACTTCA	XP_016879794.1:n.926-79_926-78insTCCTGTGACTTCA
XM_017024308.1:c.872-79_872-78insTCCTGTGACTTCA	XP_016879797.1:n.872-79_872-78insTCCTGTGACTTCA
XM_017024309.2:c.650-79_650-78insTCCTGTGACTTCA	XP_016879798.1:n.650-79_650-78insTCCTGTGACTTCA
XM_024450635.1:c.926-79_926-78insTCCTGTGACTTCA	XP_024306403.1:n.926-79_926-78insTCCTGTGACTTCA
XR_001752445.2:n.1430-79_1430-78insTCCTGTGACTTCA
NM_144997.7:c.872-79_872-78insTCCTGTGACTTCA MANE Select	NP_659434.2:n.872-79_872-78insTCCTGTGACTTCA
NM_001353229.2:c.926-79_926-78insTCCTGTGACTTCA	NP_001340158.1:n.926-79_926-78insTCCTGTGACTTCA
NM_001353230.2:c.872-79_872-78insTCCTGTGACTTCA	NP_001340159.1:n.872-79_872-78insTCCTGTGACTTCA
NM_001353231.2:c.872-79_872-78insTCCTGTGACTTCA	NP_001340160.1:n.872-79_872-78insTCCTGTGACTTCA