Canonical Allele Identifier: CA8416197
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2578503
ClinVar RCV Id: RCV003326279
dbSNP Id: rs757111995

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17219175dup , CM000679.2:g.17219175dup GRCh38
NC_000017.10:g.17122489dup , CM000679.1:g.17122489dup GRCh37
NC_000017.9:g.17063214dup NCBI36
NG_008001.2:g.23014dup , LRG_325:g.23014dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.906dup MANE Select ENSP00000285071.4:p.Glu303Ter
ENST00000285071.8:c.906dup ENSP00000285071.4:p.Glu303Ter
ENST00000427497.3:c.149-121dup ENSP00000394249.3:n.149-121dup
NM_144997.5:c.906dup , LRG_325t1:c.906dup NP_659434.2:p.Glu303Ter
XM_011523714.1:c.960dup XP_011522016.1:p.Glu321Ter
XM_011523715.1:c.960dup XP_011522017.1:p.Glu321Ter
XM_011523716.1:c.960dup XP_011522018.1:p.Glu321Ter
XM_011523717.1:c.960dup XP_011522019.1:p.Glu321Ter
XM_011523718.1:c.960dup XP_011522020.1:p.Glu321Ter
XM_011523719.1:c.960dup XP_011522021.1:p.Glu321Ter
XM_011523720.1:c.684dup XP_011522022.1:p.Glu229Ter
XM_011523721.1:c.960dup XP_011522023.1:p.Glu321Ter
XR_934007.1:n.2300dup
NM_001353229.1:c.960dup NP_001340158.1:p.Glu321Ter
NM_001353230.1:c.906dup NP_001340159.1:p.Glu303Ter
NM_001353231.1:c.906dup NP_001340160.1:p.Glu303Ter
NM_144997.6:c.906dup NP_659434.2:p.Glu303Ter
XM_011523714.3:c.960dup XP_011522016.1:p.Glu321Ter
XM_011523718.3:c.960dup XP_011522020.1:p.Glu321Ter
XM_011523719.3:c.960dup XP_011522021.1:p.Glu321Ter
XM_011523721.3:c.960dup XP_011522023.1:p.Glu321Ter
XM_017024305.2:c.960dup XP_016879794.1:p.Glu321Ter
XM_017024308.1:c.906dup XP_016879797.1:p.Glu303Ter
XM_017024309.2:c.684dup XP_016879798.1:p.Glu229Ter
XM_024450635.1:c.960dup XP_024306403.1:p.Glu321Ter
XR_001752445.2:n.1464dup
NM_144997.7:c.906dup MANE Select NP_659434.2:p.Glu303Ter
NM_001353229.2:c.960dup NP_001340158.1:p.Glu321Ter
NM_001353230.2:c.906dup NP_001340159.1:p.Glu303Ter
NM_001353231.2:c.906dup NP_001340160.1:p.Glu303Ter