Canonical Allele Identifier: CA2250422909

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17223932_17223937delinsTTGCCC , CM000679.2:g.17223932_17223937delinsTTGCCC	GRCh38
NC_000017.10:g.17127246_17127251delinsTTGCCC , CM000679.1:g.17127246_17127251delinsTTGCCC	GRCh37
NC_000017.9:g.17067971_17067976delinsTTGCCC	NCBI36
NG_008001.2:g.18252_18257delinsGGGCAA , LRG_325:g.18252_18257delinsGGGCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.603_608delinsGGGCAA MANE Select	ENSP00000285071.4:p.Gln201=
ENST00000285071.8:c.603_608delinsGGGCAA	ENSP00000285071.4:p.Gln201=
ENST00000389169.9:c.603_608delinsGGGCAA	ENSP00000373821.5:p.Gln201=
ENST00000417064.1:c.444_449delinsGGGCAA	ENSP00000410410.1:p.Gln148=
ENST00000427497.3:c.148+4053_148+4058delinsGGGCAA	ENSP00000394249.3:n.148+4053_148+4058deli...
ENST00000480316.1:n.569_574delinsGGGCAA
NM_144606.5:c.603_608delinsGGGCAA	NP_653207.1:p.Gln201=
NM_144997.5:c.603_608delinsGGGCAA , LRG_325t1:c.603_608delinsGGGCAA	NP_659434.2:p.Gln201=
XM_011523714.1:c.657_662delinsGGGCAA	XP_011522016.1:p.Gln219=
XM_011523715.1:c.657_662delinsGGGCAA	XP_011522017.1:p.Gln219=
XM_011523716.1:c.657_662delinsGGGCAA	XP_011522018.1:p.Gln219=
XM_011523717.1:c.657_662delinsGGGCAA	XP_011522019.1:p.Gln219=
XM_011523718.1:c.657_662delinsGGGCAA	XP_011522020.1:p.Gln219=
XM_011523719.1:c.657_662delinsGGGCAA	XP_011522021.1:p.Gln219=
XM_011523720.1:c.397-1276_397-1271delinsGGGCAA	XP_011522022.1:n.397-1276_397-1271delinsG...
XM_011523721.1:c.657_662delinsGGGCAA	XP_011522023.1:p.Gln219=
XR_934007.1:n.1997_2002delinsGGGCAA
NM_001353229.1:c.657_662delinsGGGCAA	NP_001340158.1:p.Gln219=
NM_001353230.1:c.603_608delinsGGGCAA	NP_001340159.1:p.Gln201=
NM_001353231.1:c.603_608delinsGGGCAA	NP_001340160.1:p.Gln201=
NM_144606.6:c.603_608delinsGGGCAA	NP_653207.1:p.Gln201=
NM_144997.6:c.603_608delinsGGGCAA	NP_659434.2:p.Gln201=
XM_011523714.3:c.657_662delinsGGGCAA	XP_011522016.1:p.Gln219=
XM_011523718.3:c.657_662delinsGGGCAA	XP_011522020.1:p.Gln219=
XM_011523719.3:c.657_662delinsGGGCAA	XP_011522021.1:p.Gln219=
XM_011523721.3:c.657_662delinsGGGCAA	XP_011522023.1:p.Gln219=
XM_017024305.2:c.657_662delinsGGGCAA	XP_016879794.1:p.Gln219=
XM_017024308.1:c.603_608delinsGGGCAA	XP_016879797.1:p.Gln201=
XM_017024309.2:c.397-1276_397-1271delinsGGGCAA	XP_016879798.1:n.397-1276_397-1271delinsG...
XM_024450635.1:c.657_662delinsGGGCAA	XP_024306403.1:p.Gln219=
XR_001752445.2:n.1161_1166delinsGGGCAA
NM_144997.7:c.603_608delinsGGGCAA MANE Select	NP_659434.2:p.Gln201=
NM_001353229.2:c.657_662delinsGGGCAA	NP_001340158.1:p.Gln219=
NM_001353230.2:c.603_608delinsGGGCAA	NP_001340159.1:p.Gln201=
NM_001353231.2:c.603_608delinsGGGCAA	NP_001340160.1:p.Gln201=
NM_144606.7:c.603_608delinsGGGCAA	NP_653207.1:p.Gln201=