Canonical Allele Identifier: CA625314018

Gene: FLCN MPRIP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17215102_17215112del , CM000679.2:g.17215102_17215112del	GRCh38
NC_000017.10:g.17118416_17118426del , CM000679.1:g.17118416_17118426del	GRCh37
NC_000017.9:g.17059141_17059151del	NCBI36
NG_008001.2:g.27079_27089del , LRG_325:g.27079_27089del

Transcript Alleles

HGVS	Amino-acid Change
NM_144997.7:c.1433-20_1433-10del (FLCN) MANE Select	NP_659434.2:n.1433-20_1433-10del
ENST00000285071.9:c.1433-20_1433-10del (FLCN) MANE Select	ENSP00000285071.4:n.1433-20_1433-10del
NM_001353229.1:c.1487-20_1487-10del (FLCN)	NP_001340158.1:n.1487-20_1487-10del
NM_001353229.2:c.1487-20_1487-10del (FLCN)	NP_001340158.1:n.1487-20_1487-10del
NM_001353230.1:c.1433-20_1433-10del (FLCN)	NP_001340159.1:n.1433-20_1433-10del
NM_001353230.2:c.1433-20_1433-10del (FLCN)	NP_001340159.1:n.1433-20_1433-10del
NM_001353231.1:c.1433-20_1433-10del (FLCN)	NP_001340160.1:n.1433-20_1433-10del
NM_001353231.2:c.1433-20_1433-10del (FLCN)	NP_001340160.1:n.1433-20_1433-10del
NM_144997.5:c.1433-20_1433-10del , LRG_325t1:c.1433-20_1433-10del (FLCN)	NP_659434.2:n.1433-20_1433-10del
NM_144997.6:c.1433-20_1433-10del (FLCN)	NP_659434.2:n.1433-20_1433-10del
ENST00000285071.8:c.1433-20_1433-10del (FLCN)	ENSP00000285071.4:n.1433-20_1433-10del
ENST00000427497.3:c.*267-20_*267-10del	ENSP00000394249.3:n.*267-20_*267-10del
ENST00000578209.5:c.562-2388_562-2378del (MPRIP)
XM_011523714.1:c.1487-20_1487-10del (FLCN)	XP_011522016.1:n.1487-20_1487-10del
XM_011523714.3:c.1487-20_1487-10del (FLCN)	XP_011522016.1:n.1487-20_1487-10del
XM_011523715.1:c.1487-20_1487-10del (FLCN)	XP_011522017.1:n.1487-20_1487-10del
XM_011523716.1:c.1487-20_1487-10del (FLCN)	XP_011522018.1:n.1487-20_1487-10del
XM_011523717.1:c.1487-20_1487-10del (FLCN)	XP_011522019.1:n.1487-20_1487-10del
XM_011523718.1:c.1487-20_1487-10del (FLCN)	XP_011522020.1:n.1487-20_1487-10del
XM_011523718.3:c.1487-20_1487-10del (FLCN)	XP_011522020.1:n.1487-20_1487-10del
XM_011523719.1:c.1487-20_1487-10del (FLCN)	XP_011522021.1:n.1487-20_1487-10del
XM_011523719.3:c.1487-20_1487-10del (FLCN)	XP_011522021.1:n.1487-20_1487-10del
XM_011523720.1:c.1211-20_1211-10del (FLCN)	XP_011522022.1:n.1211-20_1211-10del
XM_011523721.1:c.1487-20_1487-10del (FLCN)	XP_011522023.1:n.1487-20_1487-10del
XM_011523721.3:c.1487-20_1487-10del (FLCN)	XP_011522023.1:n.1487-20_1487-10del
XM_017024305.2:c.1487-20_1487-10del (FLCN)	XP_016879794.1:n.1487-20_1487-10del
XM_017024308.1:c.1433-20_1433-10del (FLCN)	XP_016879797.1:n.1433-20_1433-10del
XM_017024309.2:c.1211-20_1211-10del (FLCN)	XP_016879798.1:n.1211-20_1211-10del
XM_024450635.1:c.1487-20_1487-10del (FLCN)	XP_024306403.1:n.1487-20_1487-10del
XR_001752445.2:n.1867-20_1867-10del (FLCN)
XR_934007.1:n.2703-20_2703-10del (FLCN)