Canonical Allele Identifier: CA2573153103

Gene: FLCN

Linked Data

• ClinVar Variation Id: 1654956
• ClinVar RCV Id: RCV002156443
• dbSNP Id: rs2144947275

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17222482A>C , CM000679.2:g.17222482A>C	GRCh38
NC_000017.10:g.17125796A>C , CM000679.1:g.17125796A>C	GRCh37
NC_000017.9:g.17066521A>C	NCBI36
NG_008001.2:g.19707T>G , LRG_325:g.19707T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.779+19T>G MANE Select	ENSP00000285071.4:n.779+19T>G
ENST00000285071.8:c.779+19T>G	ENSP00000285071.4:n.779+19T>G
ENST00000389169.9:c.779+19T>G	ENSP00000373821.5:n.779+19T>G
ENST00000427497.3:c.149-3428T>G	ENSP00000394249.3:n.149-3428T>G
ENST00000466317.1:n.622+19T>G
ENST00000480316.1:n.745+19T>G
NM_144606.5:c.779+19T>G	NP_653207.1:n.779+19T>G
NM_144997.5:c.779+19T>G , LRG_325t1:c.779+19T>G	NP_659434.2:n.779+19T>G
XM_011523714.1:c.833+19T>G	XP_011522016.1:n.833+19T>G
XM_011523715.1:c.833+19T>G	XP_011522017.1:n.833+19T>G
XM_011523716.1:c.833+19T>G	XP_011522018.1:n.833+19T>G
XM_011523717.1:c.833+19T>G	XP_011522019.1:n.833+19T>G
XM_011523718.1:c.833+19T>G	XP_011522020.1:n.833+19T>G
XM_011523719.1:c.833+19T>G	XP_011522021.1:n.833+19T>G
XM_011523720.1:c.557+19T>G	XP_011522022.1:n.557+19T>G
XM_011523721.1:c.833+19T>G	XP_011522023.1:n.833+19T>G
XR_934007.1:n.2173+19T>G
NM_001353229.1:c.833+19T>G	NP_001340158.1:n.833+19T>G
NM_001353230.1:c.779+19T>G	NP_001340159.1:n.779+19T>G
NM_001353231.1:c.779+19T>G	NP_001340160.1:n.779+19T>G
NM_144606.6:c.779+19T>G	NP_653207.1:n.779+19T>G
NM_144997.6:c.779+19T>G	NP_659434.2:n.779+19T>G
XM_011523714.3:c.833+19T>G	XP_011522016.1:n.833+19T>G
XM_011523718.3:c.833+19T>G	XP_011522020.1:n.833+19T>G
XM_011523719.3:c.833+19T>G	XP_011522021.1:n.833+19T>G
XM_011523721.3:c.833+19T>G	XP_011522023.1:n.833+19T>G
XM_017024305.2:c.833+19T>G	XP_016879794.1:n.833+19T>G
XM_017024308.1:c.779+19T>G	XP_016879797.1:n.779+19T>G
XM_017024309.2:c.557+19T>G	XP_016879798.1:n.557+19T>G
XM_024450635.1:c.833+19T>G	XP_024306403.1:n.833+19T>G
XR_001752445.2:n.1337+19T>G
NM_144997.7:c.779+19T>G MANE Select	NP_659434.2:n.779+19T>G
NM_001353229.2:c.833+19T>G	NP_001340158.1:n.833+19T>G
NM_001353230.2:c.779+19T>G	NP_001340159.1:n.779+19T>G
NM_001353231.2:c.779+19T>G	NP_001340160.1:n.779+19T>G
NM_144606.7:c.779+19T>G	NP_653207.1:n.779+19T>G