Canonical Allele Identifier: CA398532150
Community Standard Title: NM_144997.7(FLCN):c.1160C>T (p.Ala387Val)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17217085G>A , CM000679.2:g.17217085G>A GRCh38
NC_000017.10:g.17120399G>A , CM000679.1:g.17120399G>A GRCh37
NC_000017.9:g.17061124G>A NCBI36
NG_008001.2:g.25104C>T , LRG_325:g.25104C>T

Transcript Alleles

HGVS Amino-acid Change
NM_144997.7:c.1160C>T (FLCN) MANE Select NP_659434.2:p.Ala387Val
ENST00000285071.9:c.1160C>T (FLCN) MANE Select ENSP00000285071.4:p.Ala387Val
NM_001353229.1:c.1214C>T (FLCN) NP_001340158.1:p.Ala405Val
NM_001353229.2:c.1214C>T (FLCN) NP_001340158.1:p.Ala405Val
NM_001353230.1:c.1160C>T (FLCN) NP_001340159.1:p.Ala387Val
NM_001353230.2:c.1160C>T (FLCN) NP_001340159.1:p.Ala387Val
NM_001353231.1:c.1160C>T (FLCN) NP_001340160.1:p.Ala387Val
NM_001353231.2:c.1160C>T (FLCN) NP_001340160.1:p.Ala387Val
NM_144997.5:c.1160C>T , LRG_325t1:c.1160C>T (FLCN) NP_659434.2:p.Ala387Val
NM_144997.6:c.1160C>T (FLCN) NP_659434.2:p.Ala387Val
ENST00000285071.8:c.1160C>T (FLCN) ENSP00000285071.4:p.Ala387Val
ENST00000427497.3:c.282C>T ENSP00000394249.3:p.Ser94=
ENST00000577591.1:n.183C>T (FLCN)
ENST00000578209.5:c.562-405G>A (MPRIP)
XM_011523714.1:c.1214C>T (FLCN) XP_011522016.1:p.Ala405Val
XM_011523714.3:c.1214C>T (FLCN) XP_011522016.1:p.Ala405Val
XM_011523715.1:c.1214C>T (FLCN) XP_011522017.1:p.Ala405Val
XM_011523716.1:c.1214C>T (FLCN) XP_011522018.1:p.Ala405Val
XM_011523717.1:c.1214C>T (FLCN) XP_011522019.1:p.Ala405Val
XM_011523718.1:c.1214C>T (FLCN) XP_011522020.1:p.Ala405Val
XM_011523718.3:c.1214C>T (FLCN) XP_011522020.1:p.Ala405Val
XM_011523719.1:c.1214C>T (FLCN) XP_011522021.1:p.Ala405Val
XM_011523719.3:c.1214C>T (FLCN) XP_011522021.1:p.Ala405Val
XM_011523720.1:c.938C>T (FLCN) XP_011522022.1:p.Ala313Val
XM_011523721.1:c.1214C>T (FLCN) XP_011522023.1:p.Ala405Val
XM_011523721.3:c.1214C>T (FLCN) XP_011522023.1:p.Ala405Val
XM_017024305.2:c.1214C>T (FLCN) XP_016879794.1:p.Ala405Val
XM_017024308.1:c.1160C>T (FLCN) XP_016879797.1:p.Ala387Val
XM_017024309.2:c.938C>T (FLCN) XP_016879798.1:p.Ala313Val
XM_024450635.1:c.1214C>T (FLCN) XP_024306403.1:p.Ala405Val
XR_001752445.2:n.1718C>T (FLCN)
XR_934007.1:n.2554C>T (FLCN)