Canonical Allele Identifier: CA2636350793

Gene: FLCN MPRIP

Linked Data

• gnomAD v4: 17-17216655-GGGGGTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17216660_17216666del , CM000679.2:g.17216660_17216666del	GRCh38
NC_000017.10:g.17119974_17119980del , CM000679.1:g.17119974_17119980del	GRCh37
NC_000017.9:g.17060699_17060705del	NCBI36
NG_008001.2:g.25527_25533del , LRG_325:g.25527_25533del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1177-159_1177-153del (FLCN) MANE Select	ENSP00000285071.4:n.1177-159_1177-153del
ENST00000285071.8:c.1177-159_1177-153del (FLCN)	ENSP00000285071.4:n.1177-159_1177-153del
ENST00000427497.3:c.*11-159_*11-153del	ENSP00000394249.3:n.*11-159_*11-153del
ENST00000578209.5:c.562-830_562-824del (MPRIP)
NM_144997.5:c.1177-159_1177-153del , LRG_325t1:c.1177-159_1177-153del (FLCN)	NP_659434.2:n.1177-159_1177-153del
XM_011523714.1:c.1231-159_1231-153del (FLCN)	XP_011522016.1:n.1231-159_1231-153del
XM_011523715.1:c.1231-159_1231-153del (FLCN)	XP_011522017.1:n.1231-159_1231-153del
XM_011523716.1:c.1231-159_1231-153del (FLCN)	XP_011522018.1:n.1231-159_1231-153del
XM_011523717.1:c.1231-159_1231-153del (FLCN)	XP_011522019.1:n.1231-159_1231-153del
XM_011523718.1:c.1231-159_1231-153del (FLCN)	XP_011522020.1:n.1231-159_1231-153del
XM_011523719.1:c.1231-159_1231-153del (FLCN)	XP_011522021.1:n.1231-159_1231-153del
XM_011523720.1:c.955-159_955-153del (FLCN)	XP_011522022.1:n.955-159_955-153del
XM_011523721.1:c.1231-159_1231-153del (FLCN)	XP_011522023.1:n.1231-159_1231-153del
XR_934007.1:n.2570+407_2570+413del (FLCN)
NM_001353229.1:c.1231-159_1231-153del (FLCN)	NP_001340158.1:n.1231-159_1231-153del
NM_001353230.1:c.1177-159_1177-153del (FLCN)	NP_001340159.1:n.1177-159_1177-153del
NM_001353231.1:c.1177-159_1177-153del (FLCN)	NP_001340160.1:n.1177-159_1177-153del
NM_144997.6:c.1177-159_1177-153del (FLCN)	NP_659434.2:n.1177-159_1177-153del
XM_011523714.3:c.1231-159_1231-153del (FLCN)	XP_011522016.1:n.1231-159_1231-153del
XM_011523718.3:c.1231-159_1231-153del (FLCN)	XP_011522020.1:n.1231-159_1231-153del
XM_011523719.3:c.1231-159_1231-153del (FLCN)	XP_011522021.1:n.1231-159_1231-153del
XM_011523721.3:c.1231-159_1231-153del (FLCN)	XP_011522023.1:n.1231-159_1231-153del
XM_017024305.2:c.1231-159_1231-153del (FLCN)	XP_016879794.1:n.1231-159_1231-153del
XM_017024308.1:c.1177-159_1177-153del (FLCN)	XP_016879797.1:n.1177-159_1177-153del
XM_017024309.2:c.955-159_955-153del (FLCN)	XP_016879798.1:n.955-159_955-153del
XM_024450635.1:c.1231-159_1231-153del (FLCN)	XP_024306403.1:n.1231-159_1231-153del
XR_001752445.2:n.1734+407_1734+413del (FLCN)
NM_144997.7:c.1177-159_1177-153del (FLCN) MANE Select	NP_659434.2:n.1177-159_1177-153del
NM_001353229.2:c.1231-159_1231-153del (FLCN)	NP_001340158.1:n.1231-159_1231-153del
NM_001353230.2:c.1177-159_1177-153del (FLCN)	NP_001340159.1:n.1177-159_1177-153del
NM_001353231.2:c.1177-159_1177-153del (FLCN)	NP_001340160.1:n.1177-159_1177-153del