Canonical Allele Identifier: CA2636351999

Gene: FLCN MPRIP

Linked Data

• gnomAD v4: 17-17217036-TGCGCCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17217037_17217042del , CM000679.2:g.17217037_17217042del	GRCh38
NC_000017.10:g.17120351_17120356del , CM000679.1:g.17120351_17120356del	GRCh37
NC_000017.9:g.17061076_17061081del	NCBI36
NG_008001.2:g.25147_25152del , LRG_325:g.25147_25152del

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.1176+27_1176+32del (FLCN) MANE Select	ENSP00000285071.4:n.1176+27_1176+32del
ENST00000285071.8:c.1176+27_1176+32del (FLCN)	ENSP00000285071.4:n.1176+27_1176+32del
ENST00000427497.3:c.*10+27_*10+32del	ENSP00000394249.3:n.*10+27_*10+32del
ENST00000577591.1:n.226_231del (FLCN)
ENST00000578209.5:c.562-453_562-448del (MPRIP)
NM_144997.5:c.1176+27_1176+32del , LRG_325t1:c.1176+27_1176+32del (FLCN)	NP_659434.2:n.1176+27_1176+32del
XM_011523714.1:c.1230+27_1230+32del (FLCN)	XP_011522016.1:n.1230+27_1230+32del
XM_011523715.1:c.1230+27_1230+32del (FLCN)	XP_011522017.1:n.1230+27_1230+32del
XM_011523716.1:c.1230+27_1230+32del (FLCN)	XP_011522018.1:n.1230+27_1230+32del
XM_011523717.1:c.1230+27_1230+32del (FLCN)	XP_011522019.1:n.1230+27_1230+32del
XM_011523718.1:c.1230+27_1230+32del (FLCN)	XP_011522020.1:n.1230+27_1230+32del
XM_011523719.1:c.1230+27_1230+32del (FLCN)	XP_011522021.1:n.1230+27_1230+32del
XM_011523720.1:c.954+27_954+32del (FLCN)	XP_011522022.1:n.954+27_954+32del
XM_011523721.1:c.1230+27_1230+32del (FLCN)	XP_011522023.1:n.1230+27_1230+32del
XR_934007.1:n.2570+27_2570+32del (FLCN)
NM_001353229.1:c.1230+27_1230+32del (FLCN)	NP_001340158.1:n.1230+27_1230+32del
NM_001353230.1:c.1176+27_1176+32del (FLCN)	NP_001340159.1:n.1176+27_1176+32del
NM_001353231.1:c.1176+27_1176+32del (FLCN)	NP_001340160.1:n.1176+27_1176+32del
NM_144997.6:c.1176+27_1176+32del (FLCN)	NP_659434.2:n.1176+27_1176+32del
XM_011523714.3:c.1230+27_1230+32del (FLCN)	XP_011522016.1:n.1230+27_1230+32del
XM_011523718.3:c.1230+27_1230+32del (FLCN)	XP_011522020.1:n.1230+27_1230+32del
XM_011523719.3:c.1230+27_1230+32del (FLCN)	XP_011522021.1:n.1230+27_1230+32del
XM_011523721.3:c.1230+27_1230+32del (FLCN)	XP_011522023.1:n.1230+27_1230+32del
XM_017024305.2:c.1230+27_1230+32del (FLCN)	XP_016879794.1:n.1230+27_1230+32del
XM_017024308.1:c.1176+27_1176+32del (FLCN)	XP_016879797.1:n.1176+27_1176+32del
XM_017024309.2:c.954+27_954+32del (FLCN)	XP_016879798.1:n.954+27_954+32del
XM_024450635.1:c.1230+27_1230+32del (FLCN)	XP_024306403.1:n.1230+27_1230+32del
XR_001752445.2:n.1734+27_1734+32del (FLCN)
NM_144997.7:c.1176+27_1176+32del (FLCN) MANE Select	NP_659434.2:n.1176+27_1176+32del
NM_001353229.2:c.1230+27_1230+32del (FLCN)	NP_001340158.1:n.1230+27_1230+32del
NM_001353230.2:c.1176+27_1176+32del (FLCN)	NP_001340159.1:n.1176+27_1176+32del
NM_001353231.2:c.1176+27_1176+32del (FLCN)	NP_001340160.1:n.1176+27_1176+32del