Canonical Allele Identifier: CA981917516
Gene: FLCN HGNC NCBI

Linked Data

dbSNP Id: rs2047432955

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17231864C>T , CM000679.2:g.17231864C>T GRCh38
NC_000017.10:g.17135178C>T , CM000679.1:g.17135178C>T GRCh37
NC_000017.9:g.17075903C>T NCBI36
NG_008001.2:g.10325G>A , LRG_325:g.10325G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000285071.9:c.-95G>A MANE Select ENSP00000285071.4:n.-95G>A
ENST00000285071.8:c.-95G>A ENSP00000285071.4:n.-95G>A
ENST00000389169.9:c.-95G>A ENSP00000373821.5:n.-95G>A
ENST00000389171.4:n.410G>A
ENST00000417064.1:c.-27-3859G>A ENSP00000410410.1:n.-27-3859G>A
ENST00000427497.3:c.-95G>A ENSP00000394249.3:n.-95G>A
ENST00000473853.1:n.44G>A
NM_144606.5:c.-95G>A NP_653207.1:n.-95G>A
NM_144997.5:c.-95G>A , LRG_325t1:c.-95G>A NP_659434.2:n.-95G>A
XM_011523714.1:c.-95G>A XP_011522016.1:n.-95G>A
XM_011523715.1:c.-839G>A XP_011522017.1:n.-839G>A
XM_011523717.1:c.-755G>A XP_011522019.1:n.-755G>A
XM_011523718.1:c.-25+924G>A XP_011522020.1:n.-25+924G>A
XM_011523721.1:c.-25+924G>A XP_011522023.1:n.-25+924G>A
NM_001353229.1:c.-95G>A NP_001340158.1:n.-95G>A
NM_001353230.1:c.-378G>A NP_001340159.1:n.-378G>A
NM_001353231.1:c.-294G>A NP_001340160.1:n.-294G>A
NM_144606.6:c.-95G>A NP_653207.1:n.-95G>A
NM_144997.6:c.-95G>A NP_659434.2:n.-95G>A
XM_011523714.3:c.-95G>A XP_011522016.1:n.-95G>A
XM_011523718.3:c.-25+924G>A XP_011522020.1:n.-25+924G>A
XM_011523719.3:c.-95G>A XP_011522021.1:n.-95G>A
XM_011523721.3:c.-25+924G>A XP_011522023.1:n.-25+924G>A
XM_017024305.2:c.-294G>A XP_016879794.1:n.-294G>A
XM_017024308.1:c.-294G>A XP_016879797.1:n.-294G>A
XM_017024309.2:c.-95G>A XP_016879798.1:n.-95G>A
XM_024450635.1:c.-1303G>A XP_024306403.1:n.-1303G>A
XR_001752445.2:n.410G>A
NM_144997.7:c.-95G>A MANE Select NP_659434.2:n.-95G>A
NM_001353229.2:c.-95G>A NP_001340158.1:n.-95G>A
NM_001353230.2:c.-378G>A NP_001340159.1:n.-378G>A
NM_001353231.2:c.-294G>A NP_001340160.1:n.-294G>A
NM_144606.7:c.-95G>A NP_653207.1:n.-95G>A