Canonical Allele Identifier: CA2250421188

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17222615A= , CM000679.2:g.17222615A=	GRCh38
NC_000017.10:g.17125929A= , CM000679.1:g.17125929A=	GRCh37
NC_000017.9:g.17066654A=	NCBI36
NG_008001.2:g.19574T= , LRG_325:g.19574T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.665T= MANE Select	ENSP00000285071.4:p.Met222=
ENST00000285071.8:c.665T=	ENSP00000285071.4:p.Met222=
ENST00000389169.9:c.665T=	ENSP00000373821.5:p.Met222=
ENST00000427497.3:c.149-3561T=	ENSP00000394249.3:n.149-3561T=
ENST00000466317.1:n.508T=
ENST00000480316.1:n.631T=
NM_144606.5:c.665T=	NP_653207.1:p.Met222=
NM_144997.5:c.665T= , LRG_325t1:c.665T=	NP_659434.2:p.Met222=
XM_011523714.1:c.719T=	XP_011522016.1:p.Met240=
XM_011523715.1:c.719T=	XP_011522017.1:p.Met240=
XM_011523716.1:c.719T=	XP_011522018.1:p.Met240=
XM_011523717.1:c.719T=	XP_011522019.1:p.Met240=
XM_011523718.1:c.719T=	XP_011522020.1:p.Met240=
XM_011523719.1:c.719T=	XP_011522021.1:p.Met240=
XM_011523720.1:c.443T=	XP_011522022.1:p.Met148=
XM_011523721.1:c.719T=	XP_011522023.1:p.Met240=
XR_934007.1:n.2059T=
NM_001353229.1:c.719T=	NP_001340158.1:p.Met240=
NM_001353230.1:c.665T=	NP_001340159.1:p.Met222=
NM_001353231.1:c.665T=	NP_001340160.1:p.Met222=
NM_144606.6:c.665T=	NP_653207.1:p.Met222=
NM_144997.6:c.665T=	NP_659434.2:p.Met222=
XM_011523714.3:c.719T=	XP_011522016.1:p.Met240=
XM_011523718.3:c.719T=	XP_011522020.1:p.Met240=
XM_011523719.3:c.719T=	XP_011522021.1:p.Met240=
XM_011523721.3:c.719T=	XP_011522023.1:p.Met240=
XM_017024305.2:c.719T=	XP_016879794.1:p.Met240=
XM_017024308.1:c.665T=	XP_016879797.1:p.Met222=
XM_017024309.2:c.443T=	XP_016879798.1:p.Met148=
XM_024450635.1:c.719T=	XP_024306403.1:p.Met240=
XR_001752445.2:n.1223T=
NM_144997.7:c.665T= MANE Select	NP_659434.2:p.Met222=
NM_001353229.2:c.719T=	NP_001340158.1:p.Met240=
NM_001353230.2:c.665T=	NP_001340159.1:p.Met222=
NM_001353231.2:c.665T=	NP_001340160.1:p.Met222=
NM_144606.7:c.665T=	NP_653207.1:p.Met222=