Canonical Allele Identifier: CA2636351977

Gene: FLCN MPRIP

Linked Data

• gnomAD v4: 17-17217029-A-ATTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217029_17217030insTTG , CM000679.2:g.17217029_17217030insTTG	GRCh38
NC_000017.10:g.17120343_17120344insTTG , CM000679.1:g.17120343_17120344insTTG	GRCh37
NC_000017.9:g.17061068_17061069insTTG	NCBI36
NG_008001.2:g.25159_25160insCAA , LRG_325:g.25159_25160insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1176+39_1176+40insCAA (FLCN) MANE Select	ENSP00000285071.4:n.1176+39_1176+40insCAA
ENST00000285071.8:c.1176+39_1176+40insCAA (FLCN)	ENSP00000285071.4:n.1176+39_1176+40insCAA
ENST00000427497.3:c.*10+39_*10+40insCAA	ENSP00000394249.3:n.*10+39_*10+40insCAA
ENST00000577591.1:n.238_239insCAA (FLCN)
ENST00000578209.5:c.562-461_562-460insTTG (MPRIP)
NM_144997.5:c.1176+39_1176+40insCAA , LRG_325t1:c.1176+39_1176+40insCAA (FLCN)	NP_659434.2:n.1176+39_1176+40insCAA
XM_011523714.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522016.1:n.1230+39_1230+40insCAA
XM_011523715.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522017.1:n.1230+39_1230+40insCAA
XM_011523716.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522018.1:n.1230+39_1230+40insCAA
XM_011523717.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522019.1:n.1230+39_1230+40insCAA
XM_011523718.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522020.1:n.1230+39_1230+40insCAA
XM_011523719.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522021.1:n.1230+39_1230+40insCAA
XM_011523720.1:c.954+39_954+40insCAA (FLCN)	XP_011522022.1:n.954+39_954+40insCAA
XM_011523721.1:c.1230+39_1230+40insCAA (FLCN)	XP_011522023.1:n.1230+39_1230+40insCAA
XR_934007.1:n.2570+39_2570+40insCAA (FLCN)
NM_001353229.1:c.1230+39_1230+40insCAA (FLCN)	NP_001340158.1:n.1230+39_1230+40insCAA
NM_001353230.1:c.1176+39_1176+40insCAA (FLCN)	NP_001340159.1:n.1176+39_1176+40insCAA
NM_001353231.1:c.1176+39_1176+40insCAA (FLCN)	NP_001340160.1:n.1176+39_1176+40insCAA
NM_144997.6:c.1176+39_1176+40insCAA (FLCN)	NP_659434.2:n.1176+39_1176+40insCAA
XM_011523714.3:c.1230+39_1230+40insCAA (FLCN)	XP_011522016.1:n.1230+39_1230+40insCAA
XM_011523718.3:c.1230+39_1230+40insCAA (FLCN)	XP_011522020.1:n.1230+39_1230+40insCAA
XM_011523719.3:c.1230+39_1230+40insCAA (FLCN)	XP_011522021.1:n.1230+39_1230+40insCAA
XM_011523721.3:c.1230+39_1230+40insCAA (FLCN)	XP_011522023.1:n.1230+39_1230+40insCAA
XM_017024305.2:c.1230+39_1230+40insCAA (FLCN)	XP_016879794.1:n.1230+39_1230+40insCAA
XM_017024308.1:c.1176+39_1176+40insCAA (FLCN)	XP_016879797.1:n.1176+39_1176+40insCAA
XM_017024309.2:c.954+39_954+40insCAA (FLCN)	XP_016879798.1:n.954+39_954+40insCAA
XM_024450635.1:c.1230+39_1230+40insCAA (FLCN)	XP_024306403.1:n.1230+39_1230+40insCAA
XR_001752445.2:n.1734+39_1734+40insCAA (FLCN)
NM_144997.7:c.1176+39_1176+40insCAA (FLCN) MANE Select	NP_659434.2:n.1176+39_1176+40insCAA
NM_001353229.2:c.1230+39_1230+40insCAA (FLCN)	NP_001340158.1:n.1230+39_1230+40insCAA
NM_001353230.2:c.1176+39_1176+40insCAA (FLCN)	NP_001340159.1:n.1176+39_1176+40insCAA
NM_001353231.2:c.1176+39_1176+40insCAA (FLCN)	NP_001340160.1:n.1176+39_1176+40insCAA