Canonical Allele Identifier: CA10583454
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241931
ClinVar RCV Id: RCV000231805
dbSNP Id: rs878855220

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17221580delinsTCT , CM000679.2:g.17221580delinsTCT GRCh38
NC_000017.10:g.17124894delinsTCT , CM000679.1:g.17124894delinsTCT GRCh37
NC_000017.9:g.17065619delinsTCT NCBI36
NG_008001.2:g.20609delinsAGA , LRG_325:g.20609delinsAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000285071.9:c.828delinsAGA MANE Select ENSP00000285071.4:p.Ala277GlufsTer17
ENST00000285071.8:c.828delinsAGA ENSP00000285071.4:p.Ala277GlufsTer17
ENST00000389169.9:c.828delinsAGA ENSP00000373821.5:p.Ala277GlufsTer?
ENST00000427497.3:c.149-2526delinsAGA ENSP00000394249.3:n.149-2526delinsAGA
ENST00000466317.1:n.671delinsAGA
NM_144606.5:c.828delinsAGA NP_653207.1:p.Ala277GlufsTer?
NM_144997.5:c.828delinsAGA , LRG_325t1:c.828delinsAGA NP_659434.2:p.Ala277GlufsTer17
XM_011523714.1:c.882delinsAGA XP_011522016.1:p.Ala295GlufsTer17
XM_011523715.1:c.882delinsAGA XP_011522017.1:p.Ala295GlufsTer17
XM_011523716.1:c.882delinsAGA XP_011522018.1:p.Ala295GlufsTer17
XM_011523717.1:c.882delinsAGA XP_011522019.1:p.Ala295GlufsTer17
XM_011523718.1:c.882delinsAGA XP_011522020.1:p.Ala295GlufsTer17
XM_011523719.1:c.882delinsAGA XP_011522021.1:p.Ala295GlufsTer17
XM_011523720.1:c.606delinsAGA XP_011522022.1:p.Ala203GlufsTer17
XM_011523721.1:c.882delinsAGA XP_011522023.1:p.Ala295GlufsTer17
XR_934007.1:n.2222delinsAGA
NM_001353229.1:c.882delinsAGA NP_001340158.1:p.Ala295GlufsTer17
NM_001353230.1:c.828delinsAGA NP_001340159.1:p.Ala277GlufsTer17
NM_001353231.1:c.828delinsAGA NP_001340160.1:p.Ala277GlufsTer17
NM_144606.6:c.828delinsAGA NP_653207.1:p.Ala277GlufsTer?
NM_144997.6:c.828delinsAGA NP_659434.2:p.Ala277GlufsTer17
XM_011523714.3:c.882delinsAGA XP_011522016.1:p.Ala295GlufsTer17
XM_011523718.3:c.882delinsAGA XP_011522020.1:p.Ala295GlufsTer17
XM_011523719.3:c.882delinsAGA XP_011522021.1:p.Ala295GlufsTer17
XM_011523721.3:c.882delinsAGA XP_011522023.1:p.Ala295GlufsTer17
XM_017024305.2:c.882delinsAGA XP_016879794.1:p.Ala295GlufsTer17
XM_017024308.1:c.828delinsAGA XP_016879797.1:p.Ala277GlufsTer17
XM_017024309.2:c.606delinsAGA XP_016879798.1:p.Ala203GlufsTer17
XM_024450635.1:c.882delinsAGA XP_024306403.1:p.Ala295GlufsTer17
XR_001752445.2:n.1386delinsAGA
NM_144997.7:c.828delinsAGA MANE Select NP_659434.2:p.Ala277GlufsTer17
NM_001353229.2:c.882delinsAGA NP_001340158.1:p.Ala295GlufsTer17
NM_001353230.2:c.828delinsAGA NP_001340159.1:p.Ala277GlufsTer17
NM_001353231.2:c.828delinsAGA NP_001340160.1:p.Ala277GlufsTer17
NM_144606.7:c.828delinsAGA NP_653207.1:p.Ala277GlufsTer?