Canonical Allele Identifier: CA726585266

Gene: FLCN MPRIP

Linked Data

• dbSNP Id: rs1191135509
• gnomAD v3: 17-17216697-CTT-C
• gnomAD v4: 17-17216697-CTT-C
• MyVariant Identifiers: chr17:g.17120012_17120013del (hg19) ; chr17:g.17216698_17216699del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17216698_17216699del , CM000679.2:g.17216698_17216699del	GRCh38
NC_000017.10:g.17120012_17120013del , CM000679.1:g.17120012_17120013del	GRCh37
NC_000017.9:g.17060737_17060738del	NCBI36
NG_008001.2:g.25490_25491del , LRG_325:g.25490_25491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1177-196_1177-195del (FLCN) MANE Select	ENSP00000285071.4:n.1177-196_1177-195del
ENST00000285071.8:c.1177-196_1177-195del (FLCN)	ENSP00000285071.4:n.1177-196_1177-195del
ENST00000427497.3:c.*11-196_*11-195del	ENSP00000394249.3:n.*11-196_*11-195del
ENST00000578209.5:c.562-792_562-791del (MPRIP)
NM_144997.5:c.1177-196_1177-195del , LRG_325t1:c.1177-196_1177-195del (FLCN)	NP_659434.2:n.1177-196_1177-195del
XM_011523714.1:c.1231-196_1231-195del (FLCN)	XP_011522016.1:n.1231-196_1231-195del
XM_011523715.1:c.1231-196_1231-195del (FLCN)	XP_011522017.1:n.1231-196_1231-195del
XM_011523716.1:c.1231-196_1231-195del (FLCN)	XP_011522018.1:n.1231-196_1231-195del
XM_011523717.1:c.1231-196_1231-195del (FLCN)	XP_011522019.1:n.1231-196_1231-195del
XM_011523718.1:c.1231-196_1231-195del (FLCN)	XP_011522020.1:n.1231-196_1231-195del
XM_011523719.1:c.1231-196_1231-195del (FLCN)	XP_011522021.1:n.1231-196_1231-195del
XM_011523720.1:c.955-196_955-195del (FLCN)	XP_011522022.1:n.955-196_955-195del
XM_011523721.1:c.1231-196_1231-195del (FLCN)	XP_011522023.1:n.1231-196_1231-195del
XR_934007.1:n.2570+370_2570+371del (FLCN)
NM_001353229.1:c.1231-196_1231-195del (FLCN)	NP_001340158.1:n.1231-196_1231-195del
NM_001353230.1:c.1177-196_1177-195del (FLCN)	NP_001340159.1:n.1177-196_1177-195del
NM_001353231.1:c.1177-196_1177-195del (FLCN)	NP_001340160.1:n.1177-196_1177-195del
NM_144997.6:c.1177-196_1177-195del (FLCN)	NP_659434.2:n.1177-196_1177-195del
XM_011523714.3:c.1231-196_1231-195del (FLCN)	XP_011522016.1:n.1231-196_1231-195del
XM_011523718.3:c.1231-196_1231-195del (FLCN)	XP_011522020.1:n.1231-196_1231-195del
XM_011523719.3:c.1231-196_1231-195del (FLCN)	XP_011522021.1:n.1231-196_1231-195del
XM_011523721.3:c.1231-196_1231-195del (FLCN)	XP_011522023.1:n.1231-196_1231-195del
XM_017024305.2:c.1231-196_1231-195del (FLCN)	XP_016879794.1:n.1231-196_1231-195del
XM_017024308.1:c.1177-196_1177-195del (FLCN)	XP_016879797.1:n.1177-196_1177-195del
XM_017024309.2:c.955-196_955-195del (FLCN)	XP_016879798.1:n.955-196_955-195del
XM_024450635.1:c.1231-196_1231-195del (FLCN)	XP_024306403.1:n.1231-196_1231-195del
XR_001752445.2:n.1734+370_1734+371del (FLCN)
NM_144997.7:c.1177-196_1177-195del (FLCN) MANE Select	NP_659434.2:n.1177-196_1177-195del
NM_001353229.2:c.1231-196_1231-195del (FLCN)	NP_001340158.1:n.1231-196_1231-195del
NM_001353230.2:c.1177-196_1177-195del (FLCN)	NP_001340159.1:n.1177-196_1177-195del
NM_001353231.2:c.1177-196_1177-195del (FLCN)	NP_001340160.1:n.1177-196_1177-195del