Canonical Allele Identifier: CA10648719
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 322084
dbSNP Id: rs138847774

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17237115G>A , CM000679.2:g.17237115G>A GRCh38
NC_000017.10:g.17140429G>A , CM000679.1:g.17140429G>A GRCh37
NC_000017.9:g.17081154G>A NCBI36
NG_008001.2:g.5074C>T , LRG_325:g.5074C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.-431C>T MANE Select ENSP00000285071.4:n.-431C>T
ENST00000285071.8:c.-431C>T ENSP00000285071.4:n.-431C>T
ENST00000389169.9:c.-431C>T ENSP00000373821.5:n.-431C>T
ENST00000389171.4:n.74C>T
ENST00000417064.1:c.-231C>T ENSP00000410410.1:n.-231C>T
ENST00000427497.3:c.-431C>T ENSP00000394249.3:n.-431C>T
NM_144606.5:c.-431C>T NP_653207.1:n.-431C>T
NM_144997.5:c.-431C>T , LRG_325t1:c.-431C>T NP_659434.2:n.-431C>T
XM_011523714.1:c.-431C>T XP_011522016.1:n.-431C>T
XM_011523715.1:c.-1175C>T XP_011522017.1:n.-1175C>T
XM_011523717.1:c.-1091C>T XP_011522019.1:n.-1091C>T
XM_011523718.1:c.-342C>T XP_011522020.1:n.-342C>T
NM_001353229.1:c.-639C>T NP_001340158.1:n.-639C>T
NM_001353230.1:c.-714C>T NP_001340159.1:n.-714C>T
NM_001353231.1:c.-630C>T NP_001340160.1:n.-630C>T
NM_144606.6:c.-431C>T NP_653207.1:n.-431C>T
NM_144997.6:c.-431C>T NP_659434.2:n.-431C>T
XM_011523714.3:c.-431C>T XP_011522016.1:n.-431C>T
XM_011523718.3:c.-342C>T XP_011522020.1:n.-342C>T
XM_011523719.3:c.-431C>T XP_011522021.1:n.-431C>T
XM_017024305.2:c.-630C>T XP_016879794.1:n.-630C>T
XM_017024308.1:c.-838C>T XP_016879797.1:n.-838C>T
XM_017024309.2:c.-431C>T XP_016879798.1:n.-431C>T
XM_024450635.1:c.-1639C>T XP_024306403.1:n.-1639C>T
XR_001752445.2:n.74C>T
NM_144997.7:c.-431C>T MANE Select NP_659434.2:n.-431C>T
NM_001353229.2:c.-639C>T NP_001340158.1:n.-639C>T
NM_001353230.2:c.-714C>T NP_001340159.1:n.-714C>T
NM_001353231.2:c.-630C>T NP_001340160.1:n.-630C>T
NM_144606.7:c.-431C>T NP_653207.1:n.-431C>T