Canonical Allele Identifier: CA2250419045

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17219174_17219176delinsCAG , CM000679.2:g.17219174_17219176delinsCAG	GRCh38
NC_000017.10:g.17122488_17122490delinsCAG , CM000679.1:g.17122488_17122490delinsCAG	GRCh37
NC_000017.9:g.17063213_17063215delinsCAG	NCBI36
NG_008001.2:g.23013_23015delinsCTG , LRG_325:g.23013_23015delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.905_907delinsCTG MANE Select	ENSP00000285071.4:p.Ser302=
ENST00000285071.8:c.905_907delinsCTG	ENSP00000285071.4:p.Ser302=
ENST00000427497.3:c.149-122_149-120delinsCTG	ENSP00000394249.3:n.149-122_149-120delinsCTG
NM_144997.5:c.905_907delinsCTG , LRG_325t1:c.905_907delinsCTG	NP_659434.2:p.Ser302=
XM_011523714.1:c.959_961delinsCTG	XP_011522016.1:p.Ser320=
XM_011523715.1:c.959_961delinsCTG	XP_011522017.1:p.Ser320=
XM_011523716.1:c.959_961delinsCTG	XP_011522018.1:p.Ser320=
XM_011523717.1:c.959_961delinsCTG	XP_011522019.1:p.Ser320=
XM_011523718.1:c.959_961delinsCTG	XP_011522020.1:p.Ser320=
XM_011523719.1:c.959_961delinsCTG	XP_011522021.1:p.Ser320=
XM_011523720.1:c.683_685delinsCTG	XP_011522022.1:p.Ser228=
XM_011523721.1:c.959_961delinsCTG	XP_011522023.1:p.Ser320=
XR_934007.1:n.2299_2301delinsCTG
NM_001353229.1:c.959_961delinsCTG	NP_001340158.1:p.Ser320=
NM_001353230.1:c.905_907delinsCTG	NP_001340159.1:p.Ser302=
NM_001353231.1:c.905_907delinsCTG	NP_001340160.1:p.Ser302=
NM_144997.6:c.905_907delinsCTG	NP_659434.2:p.Ser302=
XM_011523714.3:c.959_961delinsCTG	XP_011522016.1:p.Ser320=
XM_011523718.3:c.959_961delinsCTG	XP_011522020.1:p.Ser320=
XM_011523719.3:c.959_961delinsCTG	XP_011522021.1:p.Ser320=
XM_011523721.3:c.959_961delinsCTG	XP_011522023.1:p.Ser320=
XM_017024305.2:c.959_961delinsCTG	XP_016879794.1:p.Ser320=
XM_017024308.1:c.905_907delinsCTG	XP_016879797.1:p.Ser302=
XM_017024309.2:c.683_685delinsCTG	XP_016879798.1:p.Ser228=
XM_024450635.1:c.959_961delinsCTG	XP_024306403.1:p.Ser320=
XR_001752445.2:n.1463_1465delinsCTG
NM_144997.7:c.905_907delinsCTG MANE Select	NP_659434.2:p.Ser302=
NM_001353229.2:c.959_961delinsCTG	NP_001340158.1:p.Ser320=
NM_001353230.2:c.905_907delinsCTG	NP_001340159.1:p.Ser302=
NM_001353231.2:c.905_907delinsCTG	NP_001340160.1:p.Ser302=