Canonical Allele Identifier: CA398534575
Gene: FLCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17224106T>G , CM000679.2:g.17224106T>G GRCh38
NC_000017.10:g.17127420T>G , CM000679.1:g.17127420T>G GRCh37
NC_000017.9:g.17068145T>G NCBI36
NG_008001.2:g.18083A>C , LRG_325:g.18083A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.434A>C MANE Select ENSP00000285071.4:p.Asp145Ala
ENST00000285071.8:c.434A>C ENSP00000285071.4:p.Asp145Ala
ENST00000389169.9:c.434A>C ENSP00000373821.5:p.Asp145Ala
ENST00000417064.1:c.275A>C ENSP00000410410.1:p.Asp92Ala
ENST00000427497.3:c.148+3884A>C ENSP00000394249.3:n.148+3884A>C
ENST00000480316.1:n.400A>C
NM_144606.5:c.434A>C NP_653207.1:p.Asp145Ala
NM_144997.5:c.434A>C , LRG_325t1:c.434A>C NP_659434.2:p.Asp145Ala
XM_011523714.1:c.488A>C XP_011522016.1:p.Asp163Ala
XM_011523715.1:c.488A>C XP_011522017.1:p.Asp163Ala
XM_011523716.1:c.488A>C XP_011522018.1:p.Asp163Ala
XM_011523717.1:c.488A>C XP_011522019.1:p.Asp163Ala
XM_011523718.1:c.488A>C XP_011522020.1:p.Asp163Ala
XM_011523719.1:c.488A>C XP_011522021.1:p.Asp163Ala
XM_011523720.1:c.397-1445A>C XP_011522022.1:n.397-1445A>C
XM_011523721.1:c.488A>C XP_011522023.1:p.Asp163Ala
XR_934007.1:n.1828A>C
NM_001353229.1:c.488A>C NP_001340158.1:p.Asp163Ala
NM_001353230.1:c.434A>C NP_001340159.1:p.Asp145Ala
NM_001353231.1:c.434A>C NP_001340160.1:p.Asp145Ala
NM_144606.6:c.434A>C NP_653207.1:p.Asp145Ala
NM_144997.6:c.434A>C NP_659434.2:p.Asp145Ala
XM_011523714.3:c.488A>C XP_011522016.1:p.Asp163Ala
XM_011523718.3:c.488A>C XP_011522020.1:p.Asp163Ala
XM_011523719.3:c.488A>C XP_011522021.1:p.Asp163Ala
XM_011523721.3:c.488A>C XP_011522023.1:p.Asp163Ala
XM_017024305.2:c.488A>C XP_016879794.1:p.Asp163Ala
XM_017024308.1:c.434A>C XP_016879797.1:p.Asp145Ala
XM_017024309.2:c.397-1445A>C XP_016879798.1:n.397-1445A>C
XM_024450635.1:c.488A>C XP_024306403.1:p.Asp163Ala
XR_001752445.2:n.992A>C
NM_144997.7:c.434A>C MANE Select NP_659434.2:p.Asp145Ala
NM_001353229.2:c.488A>C NP_001340158.1:p.Asp163Ala
NM_001353230.2:c.434A>C NP_001340159.1:p.Asp145Ala
NM_001353231.2:c.434A>C NP_001340160.1:p.Asp145Ala
NM_144606.7:c.434A>C NP_653207.1:p.Asp145Ala