Canonical Allele Identifier: CA16615530
Gene: FLCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17224022_17224037delinsCTGAT , CM000679.2:g.17224022_17224037delinsCTGAT GRCh38
NC_000017.10:g.17127336_17127351delinsCTGAT , CM000679.1:g.17127336_17127351delinsCTGAT GRCh37
NC_000017.9:g.17068061_17068076delinsCTGAT NCBI36
NG_008001.2:g.18152_18167delinsATCAG , LRG_325:g.18152_18167delinsATCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.503_518delinsATCAG MANE Select ENSP00000285071.4:p.Arg168HisfsTer28
ENST00000285071.8:c.503_518delinsATCAG ENSP00000285071.4:p.Arg168HisfsTer28
ENST00000389169.9:c.503_518delinsATCAG ENSP00000373821.5:p.Arg168HisfsTer28
ENST00000417064.1:c.344_359delinsATCAG ENSP00000410410.1:p.Arg115HisfsTer28
ENST00000427497.3:c.148+3953_148+3968delinsATCAG ENSP00000394249.3:n.148+3953_148+3968delinsATCAG
ENST00000480316.1:n.469_484delinsATCAG
NM_144606.5:c.503_518delinsATCAG NP_653207.1:p.Arg168HisfsTer28
NM_144997.5:c.503_518delinsATCAG , LRG_325t1:c.503_518delinsATCAG NP_659434.2:p.Arg168HisfsTer28
XM_011523714.1:c.557_572delinsATCAG XP_011522016.1:p.Arg186HisfsTer28
XM_011523715.1:c.557_572delinsATCAG XP_011522017.1:p.Arg186HisfsTer28
XM_011523716.1:c.557_572delinsATCAG XP_011522018.1:p.Arg186HisfsTer28
XM_011523717.1:c.557_572delinsATCAG XP_011522019.1:p.Arg186HisfsTer28
XM_011523718.1:c.557_572delinsATCAG XP_011522020.1:p.Arg186HisfsTer28
XM_011523719.1:c.557_572delinsATCAG XP_011522021.1:p.Arg186HisfsTer28
XM_011523720.1:c.397-1376_397-1361delinsATCAG XP_011522022.1:n.397-1376_397-1361delinsATCAG
XM_011523721.1:c.557_572delinsATCAG XP_011522023.1:p.Arg186HisfsTer28
XR_934007.1:n.1897_1912delinsATCAG
NM_001353229.1:c.557_572delinsATCAG NP_001340158.1:p.Arg186HisfsTer28
NM_001353230.1:c.503_518delinsATCAG NP_001340159.1:p.Arg168HisfsTer28
NM_001353231.1:c.503_518delinsATCAG NP_001340160.1:p.Arg168HisfsTer28
NM_144606.6:c.503_518delinsATCAG NP_653207.1:p.Arg168HisfsTer28
NM_144997.6:c.503_518delinsATCAG NP_659434.2:p.Arg168HisfsTer28
XM_011523714.3:c.557_572delinsATCAG XP_011522016.1:p.Arg186HisfsTer28
XM_011523718.3:c.557_572delinsATCAG XP_011522020.1:p.Arg186HisfsTer28
XM_011523719.3:c.557_572delinsATCAG XP_011522021.1:p.Arg186HisfsTer28
XM_011523721.3:c.557_572delinsATCAG XP_011522023.1:p.Arg186HisfsTer28
XM_017024305.2:c.557_572delinsATCAG XP_016879794.1:p.Arg186HisfsTer28
XM_017024308.1:c.503_518delinsATCAG XP_016879797.1:p.Arg168HisfsTer28
XM_017024309.2:c.397-1376_397-1361delinsATCAG XP_016879798.1:n.397-1376_397-1361delinsATCAG
XM_024450635.1:c.557_572delinsATCAG XP_024306403.1:p.Arg186HisfsTer28
XR_001752445.2:n.1061_1076delinsATCAG
NM_144997.7:c.503_518delinsATCAG MANE Select NP_659434.2:p.Arg168HisfsTer28
NM_001353229.2:c.557_572delinsATCAG NP_001340158.1:p.Arg186HisfsTer28
NM_001353230.2:c.503_518delinsATCAG NP_001340159.1:p.Arg168HisfsTer28
NM_001353231.2:c.503_518delinsATCAG NP_001340160.1:p.Arg168HisfsTer28
NM_144606.7:c.503_518delinsATCAG NP_653207.1:p.Arg168HisfsTer28