Canonical Allele Identifier: CA2250417800

Gene: FLCN MPRIP

Linked Data

• dbSNP Id: rs2046938286

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17216758_17216759insAT , CM000679.2:g.17216758_17216759insAT	GRCh38
NC_000017.10:g.17120072_17120073insAT , CM000679.1:g.17120072_17120073insAT	GRCh37
NC_000017.9:g.17060797_17060798insAT	NCBI36
NG_008001.2:g.25430_25431insAT , LRG_325:g.25430_25431insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.1177-256_1177-255insAT (FLCN) MANE Select	ENSP00000285071.4:n.1177-256_1177-255insAT
ENST00000285071.8:c.1177-256_1177-255insAT (FLCN)	ENSP00000285071.4:n.1177-256_1177-255insAT
ENST00000427497.3:c.*11-256_*11-255insAT	ENSP00000394249.3:n.*11-256_*11-255insAT
ENST00000578209.5:c.562-732_562-731insAT (MPRIP)
NM_144997.5:c.1177-256_1177-255insAT , LRG_325t1:c.1177-256_1177-255insAT (FLCN)	NP_659434.2:n.1177-256_1177-255insAT
XM_011523714.1:c.1231-256_1231-255insAT (FLCN)	XP_011522016.1:n.1231-256_1231-255insAT
XM_011523715.1:c.1231-256_1231-255insAT (FLCN)	XP_011522017.1:n.1231-256_1231-255insAT
XM_011523716.1:c.1231-256_1231-255insAT (FLCN)	XP_011522018.1:n.1231-256_1231-255insAT
XM_011523717.1:c.1231-256_1231-255insAT (FLCN)	XP_011522019.1:n.1231-256_1231-255insAT
XM_011523718.1:c.1231-256_1231-255insAT (FLCN)	XP_011522020.1:n.1231-256_1231-255insAT
XM_011523719.1:c.1231-256_1231-255insAT (FLCN)	XP_011522021.1:n.1231-256_1231-255insAT
XM_011523720.1:c.955-256_955-255insAT (FLCN)	XP_011522022.1:n.955-256_955-255insAT
XM_011523721.1:c.1231-256_1231-255insAT (FLCN)	XP_011522023.1:n.1231-256_1231-255insAT
XR_934007.1:n.2570+310_2570+311insAT (FLCN)
NM_001353229.1:c.1231-256_1231-255insAT (FLCN)	NP_001340158.1:n.1231-256_1231-255insAT
NM_001353230.1:c.1177-256_1177-255insAT (FLCN)	NP_001340159.1:n.1177-256_1177-255insAT
NM_001353231.1:c.1177-256_1177-255insAT (FLCN)	NP_001340160.1:n.1177-256_1177-255insAT
NM_144997.6:c.1177-256_1177-255insAT (FLCN)	NP_659434.2:n.1177-256_1177-255insAT
XM_011523714.3:c.1231-256_1231-255insAT (FLCN)	XP_011522016.1:n.1231-256_1231-255insAT
XM_011523718.3:c.1231-256_1231-255insAT (FLCN)	XP_011522020.1:n.1231-256_1231-255insAT
XM_011523719.3:c.1231-256_1231-255insAT (FLCN)	XP_011522021.1:n.1231-256_1231-255insAT
XM_011523721.3:c.1231-256_1231-255insAT (FLCN)	XP_011522023.1:n.1231-256_1231-255insAT
XM_017024305.2:c.1231-256_1231-255insAT (FLCN)	XP_016879794.1:n.1231-256_1231-255insAT
XM_017024308.1:c.1177-256_1177-255insAT (FLCN)	XP_016879797.1:n.1177-256_1177-255insAT
XM_017024309.2:c.955-256_955-255insAT (FLCN)	XP_016879798.1:n.955-256_955-255insAT
XM_024450635.1:c.1231-256_1231-255insAT (FLCN)	XP_024306403.1:n.1231-256_1231-255insAT
XR_001752445.2:n.1734+310_1734+311insAT (FLCN)
NM_144997.7:c.1177-256_1177-255insAT (FLCN) MANE Select	NP_659434.2:n.1177-256_1177-255insAT
NM_001353229.2:c.1231-256_1231-255insAT (FLCN)	NP_001340158.1:n.1231-256_1231-255insAT
NM_001353230.2:c.1177-256_1177-255insAT (FLCN)	NP_001340159.1:n.1177-256_1177-255insAT
NM_001353231.2:c.1177-256_1177-255insAT (FLCN)	NP_001340160.1:n.1177-256_1177-255insAT