Canonical Allele Identifier: CA2250418983
Gene: FLCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17219072_17219073delinsTC , CM000679.2:g.17219072_17219073delinsTC GRCh38
NC_000017.10:g.17122386_17122387delinsTC , CM000679.1:g.17122386_17122387delinsTC GRCh37
NC_000017.9:g.17063111_17063112delinsTC NCBI36
NG_008001.2:g.23116_23117delinsGA , LRG_325:g.23116_23117delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.1008_1009delinsGA MANE Select ENSP00000285071.4:p.Gly336=
ENST00000285071.8:c.1008_1009delinsGA ENSP00000285071.4:p.Gly336=
ENST00000427497.3:c.149-19_149-18delinsGA ENSP00000394249.3:n.149-19_149-18delinsGA
ENST00000577591.1:n.31_32delinsGA
NM_144997.5:c.1008_1009delinsGA , LRG_325t1:c.1008_1009delinsGA NP_659434.2:p.Gly336=
XM_011523714.1:c.1062_1063delinsGA XP_011522016.1:p.Gly354=
XM_011523715.1:c.1062_1063delinsGA XP_011522017.1:p.Gly354=
XM_011523716.1:c.1062_1063delinsGA XP_011522018.1:p.Gly354=
XM_011523717.1:c.1062_1063delinsGA XP_011522019.1:p.Gly354=
XM_011523718.1:c.1062_1063delinsGA XP_011522020.1:p.Gly354=
XM_011523719.1:c.1062_1063delinsGA XP_011522021.1:p.Gly354=
XM_011523720.1:c.786_787delinsGA XP_011522022.1:p.Gly262=
XM_011523721.1:c.1062_1063delinsGA XP_011522023.1:p.Gly354=
XR_934007.1:n.2402_2403delinsGA
NM_001353229.1:c.1062_1063delinsGA NP_001340158.1:p.Gly354=
NM_001353230.1:c.1008_1009delinsGA NP_001340159.1:p.Gly336=
NM_001353231.1:c.1008_1009delinsGA NP_001340160.1:p.Gly336=
NM_144997.6:c.1008_1009delinsGA NP_659434.2:p.Gly336=
XM_011523714.3:c.1062_1063delinsGA XP_011522016.1:p.Gly354=
XM_011523718.3:c.1062_1063delinsGA XP_011522020.1:p.Gly354=
XM_011523719.3:c.1062_1063delinsGA XP_011522021.1:p.Gly354=
XM_011523721.3:c.1062_1063delinsGA XP_011522023.1:p.Gly354=
XM_017024305.2:c.1062_1063delinsGA XP_016879794.1:p.Gly354=
XM_017024308.1:c.1008_1009delinsGA XP_016879797.1:p.Gly336=
XM_017024309.2:c.786_787delinsGA XP_016879798.1:p.Gly262=
XM_024450635.1:c.1062_1063delinsGA XP_024306403.1:p.Gly354=
XR_001752445.2:n.1566_1567delinsGA
NM_144997.7:c.1008_1009delinsGA MANE Select NP_659434.2:p.Gly336=
NM_001353229.2:c.1062_1063delinsGA NP_001340158.1:p.Gly354=
NM_001353230.2:c.1008_1009delinsGA NP_001340159.1:p.Gly336=
NM_001353231.2:c.1008_1009delinsGA NP_001340160.1:p.Gly336=