Canonical Allele Identifier: CA2250423604

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17224093_17224094delinsGC , CM000679.2:g.17224093_17224094delinsGC	GRCh38
NC_000017.10:g.17127407_17127408delinsGC , CM000679.1:g.17127407_17127408delinsGC	GRCh37
NC_000017.9:g.17068132_17068133delinsGC	NCBI36
NG_008001.2:g.18095_18096delinsGC , LRG_325:g.18095_18096delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.446_447delinsGC MANE Select	ENSP00000285071.4:p.Gly149=
ENST00000285071.8:c.446_447delinsGC	ENSP00000285071.4:p.Gly149=
ENST00000389169.9:c.446_447delinsGC	ENSP00000373821.5:p.Gly149=
ENST00000417064.1:c.287_288delinsGC	ENSP00000410410.1:p.Gly96=
ENST00000427497.3:c.148+3896_148+3897delinsGC	ENSP00000394249.3:n.148+3896_148+3897deli...
ENST00000480316.1:n.412_413delinsGC
NM_144606.5:c.446_447delinsGC	NP_653207.1:p.Gly149=
NM_144997.5:c.446_447delinsGC , LRG_325t1:c.446_447delinsGC	NP_659434.2:p.Gly149=
XM_011523714.1:c.500_501delinsGC	XP_011522016.1:p.Gly167=
XM_011523715.1:c.500_501delinsGC	XP_011522017.1:p.Gly167=
XM_011523716.1:c.500_501delinsGC	XP_011522018.1:p.Gly167=
XM_011523717.1:c.500_501delinsGC	XP_011522019.1:p.Gly167=
XM_011523718.1:c.500_501delinsGC	XP_011522020.1:p.Gly167=
XM_011523719.1:c.500_501delinsGC	XP_011522021.1:p.Gly167=
XM_011523720.1:c.397-1433_397-1432delinsGC	XP_011522022.1:n.397-1433_397-1432delinsG...
XM_011523721.1:c.500_501delinsGC	XP_011522023.1:p.Gly167=
XR_934007.1:n.1840_1841delinsGC
NM_001353229.1:c.500_501delinsGC	NP_001340158.1:p.Gly167=
NM_001353230.1:c.446_447delinsGC	NP_001340159.1:p.Gly149=
NM_001353231.1:c.446_447delinsGC	NP_001340160.1:p.Gly149=
NM_144606.6:c.446_447delinsGC	NP_653207.1:p.Gly149=
NM_144997.6:c.446_447delinsGC	NP_659434.2:p.Gly149=
XM_011523714.3:c.500_501delinsGC	XP_011522016.1:p.Gly167=
XM_011523718.3:c.500_501delinsGC	XP_011522020.1:p.Gly167=
XM_011523719.3:c.500_501delinsGC	XP_011522021.1:p.Gly167=
XM_011523721.3:c.500_501delinsGC	XP_011522023.1:p.Gly167=
XM_017024305.2:c.500_501delinsGC	XP_016879794.1:p.Gly167=
XM_017024308.1:c.446_447delinsGC	XP_016879797.1:p.Gly149=
XM_017024309.2:c.397-1433_397-1432delinsGC	XP_016879798.1:n.397-1433_397-1432delinsG...
XM_024450635.1:c.500_501delinsGC	XP_024306403.1:p.Gly167=
XR_001752445.2:n.1004_1005delinsGC
NM_144997.7:c.446_447delinsGC MANE Select	NP_659434.2:p.Gly149=
NM_001353229.2:c.500_501delinsGC	NP_001340158.1:p.Gly167=
NM_001353230.2:c.446_447delinsGC	NP_001340159.1:p.Gly149=
NM_001353231.2:c.446_447delinsGC	NP_001340160.1:p.Gly149=
NM_144606.7:c.446_447delinsGC	NP_653207.1:p.Gly149=