Canonical Allele Identifier: CA10648696
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322055
dbSNP Id: rs7224474

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17213299C>A , CM000679.2:g.17213299C>A GRCh38
NC_000017.10:g.17116613C>A , CM000679.1:g.17116613C>A GRCh37
NC_000017.9:g.17057338C>A NCBI36
NG_008001.2:g.28890G>T , LRG_325:g.28890G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000285071.9:c.*356G>T MANE Select ENSP00000285071.4:p.=
ENST00000285071.8:c.*356G>T ENSP00000285071.4:p.=
ENST00000427497.3:c.*372+1686G>T ENSP00000394249.3:p.=
ENST00000578209.5:n.562-4191C>A
NM_144997.5:c.*356G>T , LRG_325t1:c.*356G>T NP_659434.2:p.=
XM_011523714.1:c.*356G>T XP_011522016.1:p.=
XM_011523715.1:c.*356G>T XP_011522017.1:p.=
XM_011523716.1:c.*356G>T XP_011522018.1:p.=
XM_011523717.1:c.*356G>T XP_011522019.1:p.=
XM_011523718.1:c.*356G>T XP_011522020.1:p.=
XM_011523719.1:c.1592+1686G>T XP_011522021.1:p.=
XM_011523720.1:c.*356G>T XP_011522022.1:p.=
XM_011523721.1:c.*356G>T XP_011522023.1:p.=
NM_001353229.1:c.*356G>T NP_001340158.1:p.=
NM_001353230.1:c.*356G>T NP_001340159.1:p.=
NM_001353231.1:c.*356G>T NP_001340160.1:p.=
NM_144997.6:c.*356G>T NP_659434.2:p.=
XM_011523719.3:c.1592+1686G>T XP_011522021.1:p.=
XM_017024309.2:c.*356G>T XP_016879798.1:p.=
NM_144997.7:c.*356G>T MANE Select NP_659434.2:p.=
NM_001353229.2:c.*356G>T NP_001340158.1:p.=
NM_001353230.2:c.*356G>T NP_001340159.1:p.=
NM_001353231.2:c.*356G>T NP_001340160.1:p.=