Canonical Allele Identifier: CA2636352276

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17213416_17213417del , CM000679.2:g.17213416_17213417del GRCh38
NC_000017.10:g.17116730_17116731del , CM000679.1:g.17116730_17116731del GRCh37
NC_000017.9:g.17057455_17057456del NCBI36
NG_008001.2:g.28778_28779del , LRG_325:g.28778_28779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000285071.9:c.*244_*245del (FLCN) MANE Select ENSP00000285071.4:n.*244_*245del
ENST00000285071.8:c.*244_*245del (FLCN) ENSP00000285071.4:n.*244_*245del
ENST00000427497.3:c.*372+1574_*372+1575del ENSP00000394249.3:n.*372+1574_*372+1575del
ENST00000578209.5:c.562-4074_562-4073del (MPRIP)
NM_144997.5:c.*244_*245del , LRG_325t1:c.*244_*245del (FLCN) NP_659434.2:n.*244_*245del
XM_011523714.1:c.*244_*245del (FLCN) XP_011522016.1:n.*244_*245del
XM_011523715.1:c.*244_*245del (FLCN) XP_011522017.1:n.*244_*245del
XM_011523716.1:c.*244_*245del (FLCN) XP_011522018.1:n.*244_*245del
XM_011523717.1:c.*244_*245del (FLCN) XP_011522019.1:n.*244_*245del
XM_011523718.1:c.*244_*245del (FLCN) XP_011522020.1:n.*244_*245del
XM_011523719.1:c.1592+1574_1592+1575del (FLCN) XP_011522021.1:n.1592+1574_1592+1575del
XM_011523720.1:c.*244_*245del (FLCN) XP_011522022.1:n.*244_*245del
XM_011523721.1:c.*244_*245del (FLCN) XP_011522023.1:n.*244_*245del
NM_001353229.1:c.*244_*245del (FLCN) NP_001340158.1:n.*244_*245del
NM_001353230.1:c.*244_*245del (FLCN) NP_001340159.1:n.*244_*245del
NM_001353231.1:c.*244_*245del (FLCN) NP_001340160.1:n.*244_*245del
NM_144997.6:c.*244_*245del (FLCN) NP_659434.2:n.*244_*245del
XM_011523719.3:c.1592+1574_1592+1575del (FLCN) XP_011522021.1:n.1592+1574_1592+1575del
XM_017024309.2:c.*244_*245del (FLCN) XP_016879798.1:n.*244_*245del
NM_144997.7:c.*244_*245del (FLCN) MANE Select NP_659434.2:n.*244_*245del
NM_001353229.2:c.*244_*245del (FLCN) NP_001340158.1:n.*244_*245del
NM_001353230.2:c.*244_*245del (FLCN) NP_001340159.1:n.*244_*245del
NM_001353231.2:c.*244_*245del (FLCN) NP_001340160.1:n.*244_*245del