Canonical Allele Identifier: CA658658539

Gene: FLCN

Linked Data

• ClinVar Variation Id: 460637
• ClinVar RCV Id: RCV000543327
• dbSNP Id: rs1555608679
• MyVariant Identifiers: chr17:g.17122533_17122534del (hg19) ; chr17:g.17219219_17219220del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17219220_17219221del , CM000679.2:g.17219220_17219221del	GRCh38
NC_000017.10:g.17122534_17122535del , CM000679.1:g.17122534_17122535del	GRCh37
NC_000017.9:g.17063259_17063260del	NCBI36
NG_008001.2:g.22969_22970del , LRG_325:g.22969_22970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.872-11_872-10del MANE Select	ENSP00000285071.4:n.872-11_872-10del
ENST00000285071.8:c.872-11_872-10del	ENSP00000285071.4:n.872-11_872-10del
ENST00000427497.3:c.149-166_149-165del	ENSP00000394249.3:n.149-166_149-165del
NM_144997.5:c.872-11_872-10del , LRG_325t1:c.872-11_872-10del	NP_659434.2:n.872-11_872-10del
XM_011523714.1:c.926-11_926-10del	XP_011522016.1:n.926-11_926-10del
XM_011523715.1:c.926-11_926-10del	XP_011522017.1:n.926-11_926-10del
XM_011523716.1:c.926-11_926-10del	XP_011522018.1:n.926-11_926-10del
XM_011523717.1:c.926-11_926-10del	XP_011522019.1:n.926-11_926-10del
XM_011523718.1:c.926-11_926-10del	XP_011522020.1:n.926-11_926-10del
XM_011523719.1:c.926-11_926-10del	XP_011522021.1:n.926-11_926-10del
XM_011523720.1:c.650-11_650-10del	XP_011522022.1:n.650-11_650-10del
XM_011523721.1:c.926-11_926-10del	XP_011522023.1:n.926-11_926-10del
XR_934007.1:n.2266-11_2266-10del
NM_001353229.1:c.926-11_926-10del	NP_001340158.1:n.926-11_926-10del
NM_001353230.1:c.872-11_872-10del	NP_001340159.1:n.872-11_872-10del
NM_001353231.1:c.872-11_872-10del	NP_001340160.1:n.872-11_872-10del
NM_144997.6:c.872-11_872-10del	NP_659434.2:n.872-11_872-10del
XM_011523714.3:c.926-11_926-10del	XP_011522016.1:n.926-11_926-10del
XM_011523718.3:c.926-11_926-10del	XP_011522020.1:n.926-11_926-10del
XM_011523719.3:c.926-11_926-10del	XP_011522021.1:n.926-11_926-10del
XM_011523721.3:c.926-11_926-10del	XP_011522023.1:n.926-11_926-10del
XM_017024305.2:c.926-11_926-10del	XP_016879794.1:n.926-11_926-10del
XM_017024308.1:c.872-11_872-10del	XP_016879797.1:n.872-11_872-10del
XM_017024309.2:c.650-11_650-10del	XP_016879798.1:n.650-11_650-10del
XM_024450635.1:c.926-11_926-10del	XP_024306403.1:n.926-11_926-10del
XR_001752445.2:n.1430-11_1430-10del
NM_144997.7:c.872-11_872-10del MANE Select	NP_659434.2:n.872-11_872-10del
NM_001353229.2:c.926-11_926-10del	NP_001340158.1:n.926-11_926-10del
NM_001353230.2:c.872-11_872-10del	NP_001340159.1:n.872-11_872-10del
NM_001353231.2:c.872-11_872-10del	NP_001340160.1:n.872-11_872-10del