Canonical Allele Identifier: CA2636354612
Gene: FLCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17219152dup , CM000679.2:g.17219152dup GRCh38
NC_000017.10:g.17122466dup , CM000679.1:g.17122466dup GRCh37
NC_000017.9:g.17063191dup NCBI36
NG_008001.2:g.23040dup , LRG_325:g.23040dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.932dup MANE Select ENSP00000285071.4:p.Val312CysfsTer?
ENST00000285071.8:c.932dup ENSP00000285071.4:p.Val312CysfsTer?
ENST00000427497.3:c.149-95dup ENSP00000394249.3:n.149-95dup
NM_144997.5:c.932dup , LRG_325t1:c.932dup NP_659434.2:p.Val312CysfsTer?
XM_011523714.1:c.986dup XP_011522016.1:p.Val330CysfsTer?
XM_011523715.1:c.986dup XP_011522017.1:p.Val330CysfsTer?
XM_011523716.1:c.986dup XP_011522018.1:p.Val330CysfsTer?
XM_011523717.1:c.986dup XP_011522019.1:p.Val330CysfsTer?
XM_011523718.1:c.986dup XP_011522020.1:p.Val330CysfsTer?
XM_011523719.1:c.986dup XP_011522021.1:p.Val330CysfsTer?
XM_011523720.1:c.710dup XP_011522022.1:p.Val238CysfsTer?
XM_011523721.1:c.986dup XP_011522023.1:p.Val330CysfsTer?
XR_934007.1:n.2326dup
NM_001353229.1:c.986dup NP_001340158.1:p.Val330CysfsTer?
NM_001353230.1:c.932dup NP_001340159.1:p.Val312CysfsTer?
NM_001353231.1:c.932dup NP_001340160.1:p.Val312CysfsTer?
NM_144997.6:c.932dup NP_659434.2:p.Val312CysfsTer?
XM_011523714.3:c.986dup XP_011522016.1:p.Val330CysfsTer?
XM_011523718.3:c.986dup XP_011522020.1:p.Val330CysfsTer?
XM_011523719.3:c.986dup XP_011522021.1:p.Val330CysfsTer?
XM_011523721.3:c.986dup XP_011522023.1:p.Val330CysfsTer?
XM_017024305.2:c.986dup XP_016879794.1:p.Val330CysfsTer?
XM_017024308.1:c.932dup XP_016879797.1:p.Val312CysfsTer?
XM_017024309.2:c.710dup XP_016879798.1:p.Val238CysfsTer?
XM_024450635.1:c.986dup XP_024306403.1:p.Val330CysfsTer?
XR_001752445.2:n.1490dup
NM_144997.7:c.932dup MANE Select NP_659434.2:p.Val312CysfsTer?
NM_001353229.2:c.986dup NP_001340158.1:p.Val330CysfsTer?
NM_001353230.2:c.932dup NP_001340159.1:p.Val312CysfsTer?
NM_001353231.2:c.932dup NP_001340160.1:p.Val312CysfsTer?