Canonical Allele Identifier: CA398532283

Gene: FLCN MPRIP

Linked Data

• MyVariant Identifiers: chr17:g.17120438A>C (hg19) ; chr17:g.17217124A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217124A>C , CM000679.2:g.17217124A>C	GRCh38
NC_000017.10:g.17120438A>C , CM000679.1:g.17120438A>C	GRCh37
NC_000017.9:g.17061163A>C	NCBI36
NG_008001.2:g.25065T>G , LRG_325:g.25065T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1121T>G (FLCN) MANE Select	ENSP00000285071.4:p.Val374Gly
ENST00000285071.8:c.1121T>G (FLCN)	ENSP00000285071.4:p.Val374Gly
ENST00000427497.3:c.243T>G	ENSP00000394249.3:p.Gly81=
ENST00000577591.1:n.144T>G (FLCN)
ENST00000578209.5:c.562-366A>C (MPRIP)
NM_144997.5:c.1121T>G , LRG_325t1:c.1121T>G (FLCN)	NP_659434.2:p.Val374Gly
XM_011523714.1:c.1175T>G (FLCN)	XP_011522016.1:p.Val392Gly
XM_011523715.1:c.1175T>G (FLCN)	XP_011522017.1:p.Val392Gly
XM_011523716.1:c.1175T>G (FLCN)	XP_011522018.1:p.Val392Gly
XM_011523717.1:c.1175T>G (FLCN)	XP_011522019.1:p.Val392Gly
XM_011523718.1:c.1175T>G (FLCN)	XP_011522020.1:p.Val392Gly
XM_011523719.1:c.1175T>G (FLCN)	XP_011522021.1:p.Val392Gly
XM_011523720.1:c.899T>G (FLCN)	XP_011522022.1:p.Val300Gly
XM_011523721.1:c.1175T>G (FLCN)	XP_011522023.1:p.Val392Gly
XR_934007.1:n.2515T>G (FLCN)
NM_001353229.1:c.1175T>G (FLCN)	NP_001340158.1:p.Val392Gly
NM_001353230.1:c.1121T>G (FLCN)	NP_001340159.1:p.Val374Gly
NM_001353231.1:c.1121T>G (FLCN)	NP_001340160.1:p.Val374Gly
NM_144997.6:c.1121T>G (FLCN)	NP_659434.2:p.Val374Gly
XM_011523714.3:c.1175T>G (FLCN)	XP_011522016.1:p.Val392Gly
XM_011523718.3:c.1175T>G (FLCN)	XP_011522020.1:p.Val392Gly
XM_011523719.3:c.1175T>G (FLCN)	XP_011522021.1:p.Val392Gly
XM_011523721.3:c.1175T>G (FLCN)	XP_011522023.1:p.Val392Gly
XM_017024305.2:c.1175T>G (FLCN)	XP_016879794.1:p.Val392Gly
XM_017024308.1:c.1121T>G (FLCN)	XP_016879797.1:p.Val374Gly
XM_017024309.2:c.899T>G (FLCN)	XP_016879798.1:p.Val300Gly
XM_024450635.1:c.1175T>G (FLCN)	XP_024306403.1:p.Val392Gly
XR_001752445.2:n.1679T>G (FLCN)
NM_144997.7:c.1121T>G (FLCN) MANE Select	NP_659434.2:p.Val374Gly
NM_001353229.2:c.1175T>G (FLCN)	NP_001340158.1:p.Val392Gly
NM_001353230.2:c.1121T>G (FLCN)	NP_001340159.1:p.Val374Gly
NM_001353231.2:c.1121T>G (FLCN)	NP_001340160.1:p.Val374Gly