Canonical Allele Identifier: CA2250418930

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17218978_17218979delinsCT , CM000679.2:g.17218978_17218979delinsCT	GRCh38
NC_000017.10:g.17122292_17122293delinsCT , CM000679.1:g.17122292_17122293delinsCT	GRCh37
NC_000017.9:g.17063017_17063018delinsCT	NCBI36
NG_008001.2:g.23210_23211delinsAG , LRG_325:g.23210_23211delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.1062+40_1062+41delinsAG MANE Select	ENSP00000285071.4:n.1062+40_1062+41delins...
ENST00000285071.8:c.1062+40_1062+41delinsAG	ENSP00000285071.4:n.1062+40_1062+41delins...
ENST00000427497.3:c.184+40_184+41delinsAG	ENSP00000394249.3:n.184+40_184+41delinsAG...
ENST00000577591.1:n.85+40_85+41delinsAG
NM_144997.5:c.1062+40_1062+41delinsAG , LRG_325t1:c.1062+40_1062+41delinsAG	NP_659434.2:n.1062+40_1062+41delinsAG
XM_011523714.1:c.1116+40_1116+41delinsAG	XP_011522016.1:n.1116+40_1116+41delinsAG
XM_011523715.1:c.1116+40_1116+41delinsAG	XP_011522017.1:n.1116+40_1116+41delinsAG
XM_011523716.1:c.1116+40_1116+41delinsAG	XP_011522018.1:n.1116+40_1116+41delinsAG
XM_011523717.1:c.1116+40_1116+41delinsAG	XP_011522019.1:n.1116+40_1116+41delinsAG
XM_011523718.1:c.1116+40_1116+41delinsAG	XP_011522020.1:n.1116+40_1116+41delinsAG
XM_011523719.1:c.1116+40_1116+41delinsAG	XP_011522021.1:n.1116+40_1116+41delinsAG
XM_011523720.1:c.840+40_840+41delinsAG	XP_011522022.1:n.840+40_840+41delinsAG
XM_011523721.1:c.1116+40_1116+41delinsAG	XP_011522023.1:n.1116+40_1116+41delinsAG
XR_934007.1:n.2456+40_2456+41delinsAG
NM_001353229.1:c.1116+40_1116+41delinsAG	NP_001340158.1:n.1116+40_1116+41delinsAG
NM_001353230.1:c.1062+40_1062+41delinsAG	NP_001340159.1:n.1062+40_1062+41delinsAG
NM_001353231.1:c.1062+40_1062+41delinsAG	NP_001340160.1:n.1062+40_1062+41delinsAG
NM_144997.6:c.1062+40_1062+41delinsAG	NP_659434.2:n.1062+40_1062+41delinsAG
XM_011523714.3:c.1116+40_1116+41delinsAG	XP_011522016.1:n.1116+40_1116+41delinsAG
XM_011523718.3:c.1116+40_1116+41delinsAG	XP_011522020.1:n.1116+40_1116+41delinsAG
XM_011523719.3:c.1116+40_1116+41delinsAG	XP_011522021.1:n.1116+40_1116+41delinsAG
XM_011523721.3:c.1116+40_1116+41delinsAG	XP_011522023.1:n.1116+40_1116+41delinsAG
XM_017024305.2:c.1116+40_1116+41delinsAG	XP_016879794.1:n.1116+40_1116+41delinsAG
XM_017024308.1:c.1062+40_1062+41delinsAG	XP_016879797.1:n.1062+40_1062+41delinsAG
XM_017024309.2:c.840+40_840+41delinsAG	XP_016879798.1:n.840+40_840+41delinsAG
XM_024450635.1:c.1116+40_1116+41delinsAG	XP_024306403.1:n.1116+40_1116+41delinsAG
XR_001752445.2:n.1620+40_1620+41delinsAG
NM_144997.7:c.1062+40_1062+41delinsAG MANE Select	NP_659434.2:n.1062+40_1062+41delinsAG
NM_001353229.2:c.1116+40_1116+41delinsAG	NP_001340158.1:n.1116+40_1116+41delinsAG
NM_001353230.2:c.1062+40_1062+41delinsAG	NP_001340159.1:n.1062+40_1062+41delinsAG
NM_001353231.2:c.1062+40_1062+41delinsAG	NP_001340160.1:n.1062+40_1062+41delinsAG