Canonical Allele Identifier: CA398532170

Gene: FLCN MPRIP

Linked Data

• MyVariant Identifiers: chr17:g.17120404C>G (hg19) ; chr17:g.17217090C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217090C>G , CM000679.2:g.17217090C>G	GRCh38
NC_000017.10:g.17120404C>G , CM000679.1:g.17120404C>G	GRCh37
NC_000017.9:g.17061129C>G	NCBI36
NG_008001.2:g.25099G>C , LRG_325:g.25099G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1155G>C (FLCN) MANE Select	ENSP00000285071.4:p.Gln385His
ENST00000285071.8:c.1155G>C (FLCN)	ENSP00000285071.4:p.Gln385His
ENST00000427497.3:c.277G>C	ENSP00000394249.3:p.Val93Leu
ENST00000577591.1:n.178G>C (FLCN)
ENST00000578209.5:c.562-400C>G (MPRIP)
NM_144997.5:c.1155G>C , LRG_325t1:c.1155G>C (FLCN)	NP_659434.2:p.Gln385His
XM_011523714.1:c.1209G>C (FLCN)	XP_011522016.1:p.Gln403His
XM_011523715.1:c.1209G>C (FLCN)	XP_011522017.1:p.Gln403His
XM_011523716.1:c.1209G>C (FLCN)	XP_011522018.1:p.Gln403His
XM_011523717.1:c.1209G>C (FLCN)	XP_011522019.1:p.Gln403His
XM_011523718.1:c.1209G>C (FLCN)	XP_011522020.1:p.Gln403His
XM_011523719.1:c.1209G>C (FLCN)	XP_011522021.1:p.Gln403His
XM_011523720.1:c.933G>C (FLCN)	XP_011522022.1:p.Gln311His
XM_011523721.1:c.1209G>C (FLCN)	XP_011522023.1:p.Gln403His
XR_934007.1:n.2549G>C (FLCN)
NM_001353229.1:c.1209G>C (FLCN)	NP_001340158.1:p.Gln403His
NM_001353230.1:c.1155G>C (FLCN)	NP_001340159.1:p.Gln385His
NM_001353231.1:c.1155G>C (FLCN)	NP_001340160.1:p.Gln385His
NM_144997.6:c.1155G>C (FLCN)	NP_659434.2:p.Gln385His
XM_011523714.3:c.1209G>C (FLCN)	XP_011522016.1:p.Gln403His
XM_011523718.3:c.1209G>C (FLCN)	XP_011522020.1:p.Gln403His
XM_011523719.3:c.1209G>C (FLCN)	XP_011522021.1:p.Gln403His
XM_011523721.3:c.1209G>C (FLCN)	XP_011522023.1:p.Gln403His
XM_017024305.2:c.1209G>C (FLCN)	XP_016879794.1:p.Gln403His
XM_017024308.1:c.1155G>C (FLCN)	XP_016879797.1:p.Gln385His
XM_017024309.2:c.933G>C (FLCN)	XP_016879798.1:p.Gln311His
XM_024450635.1:c.1209G>C (FLCN)	XP_024306403.1:p.Gln403His
XR_001752445.2:n.1713G>C (FLCN)
NM_144997.7:c.1155G>C (FLCN) MANE Select	NP_659434.2:p.Gln385His
NM_001353229.2:c.1209G>C (FLCN)	NP_001340158.1:p.Gln403His
NM_001353230.2:c.1155G>C (FLCN)	NP_001340159.1:p.Gln385His
NM_001353231.2:c.1155G>C (FLCN)	NP_001340160.1:p.Gln385His