Canonical Allele Identifier: CA16043355

Gene: FLCN

Linked Data

• ClinVar Variation Id: 373895
• ClinVar RCV Id: RCV000258912 ; RCV000497517
• dbSNP Id: rs1555608614
• MyVariant Identifiers: chr17:g.17122462_17122463del (hg19) ; chr17:g.17219148_17219149del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17219148_17219149del , CM000679.2:g.17219148_17219149del	GRCh38
NC_000017.10:g.17122462_17122463del , CM000679.1:g.17122462_17122463del	GRCh37
NC_000017.9:g.17063187_17063188del	NCBI36
NG_008001.2:g.23040_23041del , LRG_325:g.23040_23041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.932_933del MANE Select	ENSP00000285071.4:p.Pro311ArgfsTer?
ENST00000285071.8:c.932_933del	ENSP00000285071.4:p.Pro311ArgfsTer?
ENST00000427497.3:c.149-95_149-94del	ENSP00000394249.3:n.149-95_149-94del
NM_144997.5:c.932_933del , LRG_325t1:c.932_933del	NP_659434.2:p.Pro311ArgfsTer?
XM_011523714.1:c.986_987del	XP_011522016.1:p.Pro329ArgfsTer?
XM_011523715.1:c.986_987del	XP_011522017.1:p.Pro329ArgfsTer?
XM_011523716.1:c.986_987del	XP_011522018.1:p.Pro329ArgfsTer?
XM_011523717.1:c.986_987del	XP_011522019.1:p.Pro329ArgfsTer?
XM_011523718.1:c.986_987del	XP_011522020.1:p.Pro329ArgfsTer?
XM_011523719.1:c.986_987del	XP_011522021.1:p.Pro329ArgfsTer?
XM_011523720.1:c.710_711del	XP_011522022.1:p.Pro237ArgfsTer?
XM_011523721.1:c.986_987del	XP_011522023.1:p.Pro329ArgfsTer?
XR_934007.1:n.2326_2327del
NM_001353229.1:c.986_987del	NP_001340158.1:p.Pro329ArgfsTer?
NM_001353230.1:c.932_933del	NP_001340159.1:p.Pro311ArgfsTer?
NM_001353231.1:c.932_933del	NP_001340160.1:p.Pro311ArgfsTer?
NM_144997.6:c.932_933del	NP_659434.2:p.Pro311ArgfsTer?
XM_011523714.3:c.986_987del	XP_011522016.1:p.Pro329ArgfsTer?
XM_011523718.3:c.986_987del	XP_011522020.1:p.Pro329ArgfsTer?
XM_011523719.3:c.986_987del	XP_011522021.1:p.Pro329ArgfsTer?
XM_011523721.3:c.986_987del	XP_011522023.1:p.Pro329ArgfsTer?
XM_017024305.2:c.986_987del	XP_016879794.1:p.Pro329ArgfsTer?
XM_017024308.1:c.932_933del	XP_016879797.1:p.Pro311ArgfsTer?
XM_017024309.2:c.710_711del	XP_016879798.1:p.Pro237ArgfsTer?
XM_024450635.1:c.986_987del	XP_024306403.1:p.Pro329ArgfsTer?
XR_001752445.2:n.1490_1491del
NM_144997.7:c.932_933del MANE Select	NP_659434.2:p.Pro311ArgfsTer?
NM_001353229.2:c.986_987del	NP_001340158.1:p.Pro329ArgfsTer?
NM_001353230.2:c.932_933del	NP_001340159.1:p.Pro311ArgfsTer?
NM_001353231.2:c.932_933del	NP_001340160.1:p.Pro311ArgfsTer?