Canonical Allele Identifier: CA2636352205

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17217132_17217207del , CM000679.2:g.17217132_17217207del GRCh38
NC_000017.10:g.17120446_17120521del , CM000679.1:g.17120446_17120521del GRCh37
NC_000017.9:g.17061171_17061246del NCBI36
NG_008001.2:g.24982_25057del , LRG_325:g.24982_25057del

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.1063-25_1113del (FLCN)
ENST00000285071.8:c.1063-25_1113del (FLCN)
ENST00000427497.3:c.185-25_235del
ENST00000577591.1:n.86-25_136del (FLCN)
ENST00000578209.5:c.562-358_562-283del (MPRIP)
NM_144997.5:c.1063-25_1113del , LRG_325t1:c.1063-25_1113del (FLCN)
XM_011523714.1:c.1117-25_1167del (FLCN)
XM_011523715.1:c.1117-25_1167del (FLCN)
XM_011523716.1:c.1117-25_1167del (FLCN)
XM_011523717.1:c.1117-25_1167del (FLCN)
XM_011523718.1:c.1117-25_1167del (FLCN)
XM_011523719.1:c.1117-25_1167del (FLCN)
XM_011523720.1:c.841-25_891del (FLCN)
XM_011523721.1:c.1117-25_1167del (FLCN)
XR_934007.1:n.2457-25_2507del (FLCN)
NM_001353229.1:c.1117-25_1167del (FLCN)
NM_001353230.1:c.1063-25_1113del (FLCN)
NM_001353231.1:c.1063-25_1113del (FLCN)
NM_144997.6:c.1063-25_1113del (FLCN)
XM_011523714.3:c.1117-25_1167del (FLCN)
XM_011523718.3:c.1117-25_1167del (FLCN)
XM_011523719.3:c.1117-25_1167del (FLCN)
XM_011523721.3:c.1117-25_1167del (FLCN)
XM_017024305.2:c.1117-25_1167del (FLCN)
XM_017024308.1:c.1063-25_1113del (FLCN)
XM_017024309.2:c.841-25_891del (FLCN)
XM_024450635.1:c.1117-25_1167del (FLCN)
XR_001752445.2:n.1621-25_1671del (FLCN)
NM_144997.7:c.1063-25_1113del (FLCN)
NM_001353229.2:c.1117-25_1167del (FLCN)
NM_001353230.2:c.1063-25_1113del (FLCN)
NM_001353231.2:c.1063-25_1113del (FLCN)