Canonical Allele Identifier: CA224168
Gene: FLCN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17226252_17226253delinsGTG , CM000679.2:g.17226252_17226253delinsGTG GRCh38
NC_000017.10:g.17129566_17129567delinsGTG , CM000679.1:g.17129566_17129567delinsGTG GRCh37
NC_000017.9:g.17070291_17070292delinsGTG NCBI36
NG_008001.2:g.15936_15937delinsCAC , LRG_325:g.15936_15937delinsCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.319_320delinsCAC MANE Select ENSP00000285071.4:p.Val107HisfsTer26
ENST00000285071.8:c.319_320delinsCAC ENSP00000285071.4:p.Val107HisfsTer26
ENST00000389168.6:n.1659_1660delinsCAC
ENST00000389169.9:c.319_320delinsCAC ENSP00000373821.5:p.Val107HisfsTer26
ENST00000389171.4:n.823_824delinsCAC
ENST00000417064.1:c.160_161delinsCAC ENSP00000410410.1:p.Val54HisfsTer26
ENST00000427497.3:c.148+1737_148+1738delinsCAC ENSP00000394249.3:n.148+1737_148+1738delinsCAC
NM_144606.5:c.319_320delinsCAC NP_653207.1:p.Val107HisfsTer26
NM_144997.5:c.319_320delinsCAC , LRG_325t1:c.319_320delinsCAC NP_659434.2:p.Val107HisfsTer26
XM_011523714.1:c.319_320delinsCAC XP_011522016.1:p.Val107HisfsTer26
XM_011523715.1:c.319_320delinsCAC XP_011522017.1:p.Val107HisfsTer26
XM_011523716.1:c.319_320delinsCAC XP_011522018.1:p.Val107HisfsTer26
XM_011523717.1:c.319_320delinsCAC XP_011522019.1:p.Val107HisfsTer26
XM_011523718.1:c.319_320delinsCAC XP_011522020.1:p.Val107HisfsTer26
XM_011523719.1:c.319_320delinsCAC XP_011522021.1:p.Val107HisfsTer26
XM_011523720.1:c.319_320delinsCAC XP_011522022.1:p.Val107HisfsTer26
XM_011523721.1:c.319_320delinsCAC XP_011522023.1:p.Val107HisfsTer26
XR_934007.1:n.1659_1660delinsCAC
NM_001353229.1:c.319_320delinsCAC NP_001340158.1:p.Val107HisfsTer26
NM_001353230.1:c.319_320delinsCAC NP_001340159.1:p.Val107HisfsTer26
NM_001353231.1:c.319_320delinsCAC NP_001340160.1:p.Val107HisfsTer26
NM_144606.6:c.319_320delinsCAC NP_653207.1:p.Val107HisfsTer26
NM_144997.6:c.319_320delinsCAC NP_659434.2:p.Val107HisfsTer26
XM_011523714.3:c.319_320delinsCAC XP_011522016.1:p.Val107HisfsTer26
XM_011523718.3:c.319_320delinsCAC XP_011522020.1:p.Val107HisfsTer26
XM_011523719.3:c.319_320delinsCAC XP_011522021.1:p.Val107HisfsTer26
XM_011523721.3:c.319_320delinsCAC XP_011522023.1:p.Val107HisfsTer26
XM_017024305.2:c.319_320delinsCAC XP_016879794.1:p.Val107HisfsTer26
XM_017024308.1:c.319_320delinsCAC XP_016879797.1:p.Val107HisfsTer26
XM_017024309.2:c.319_320delinsCAC XP_016879798.1:p.Val107HisfsTer26
XM_024450635.1:c.319_320delinsCAC XP_024306403.1:p.Val107HisfsTer26
XR_001752445.2:n.823_824delinsCAC
NM_144997.7:c.319_320delinsCAC MANE Select NP_659434.2:p.Val107HisfsTer26
NM_001353229.2:c.319_320delinsCAC NP_001340158.1:p.Val107HisfsTer26
NM_001353230.2:c.319_320delinsCAC NP_001340159.1:p.Val107HisfsTer26
NM_001353231.2:c.319_320delinsCAC NP_001340160.1:p.Val107HisfsTer26
NM_144606.7:c.319_320delinsCAC NP_653207.1:p.Val107HisfsTer26
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