Canonical Allele Identifier: CA915949596

Gene: FLCN MPRIP

Linked Data

• ClinVar Variation Id: 638865
• ClinVar RCV Id: RCV000791534

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17214986_17216673del , CM000679.2:g.17214986_17216673del	GRCh38
NC_000017.10:g.17118300_17119987del , CM000679.1:g.17118300_17119987del	GRCh37
NC_000017.9:g.17059025_17060712del	NCBI36
NG_008001.2:g.25517_27204del , LRG_325:g.25517_27204del

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.1177-169_1538del (FLCN)
ENST00000285071.8:c.1177-169_1538del (FLCN)
ENST00000427497.3:c.*11-169_*372del
ENST00000578209.5:c.562-2504_562-817del (MPRIP)
NM_144997.5:c.1177-169_1538del , LRG_325t1:c.1177-169_1538del (FLCN)
XM_011523714.1:c.1231-169_1592del (FLCN)
XM_011523715.1:c.1231-169_1592del (FLCN)
XM_011523716.1:c.1231-169_1592del (FLCN)
XM_011523717.1:c.1231-169_1592del (FLCN)
XM_011523718.1:c.1231-169_1592del (FLCN)
XM_011523719.1:c.1231-169_1592del (FLCN)
XM_011523720.1:c.955-169_1316del (FLCN)
XM_011523721.1:c.1231-169_1592del (FLCN)
XR_934007.1:n.2570+397_2808del (FLCN)
NM_001353229.1:c.1231-169_1592del (FLCN)
NM_001353230.1:c.1177-169_1538del (FLCN)
NM_001353231.1:c.1177-169_1538del (FLCN)
NM_144997.6:c.1177-169_1538del (FLCN)
XM_011523714.3:c.1231-169_1592del (FLCN)
XM_011523718.3:c.1231-169_1592del (FLCN)
XM_011523719.3:c.1231-169_1592del (FLCN)
XM_011523721.3:c.1231-169_1592del (FLCN)
XM_017024305.2:c.1231-169_1592del (FLCN)
XM_017024308.1:c.1177-169_1538del (FLCN)
XM_017024309.2:c.955-169_1316del (FLCN)
XM_024450635.1:c.1231-169_1592del (FLCN)
XR_001752445.2:n.1734+397_1972del (FLCN)
NM_144997.7:c.1177-169_1538del (FLCN)
NM_001353229.2:c.1231-169_1592del (FLCN)
NM_001353230.2:c.1177-169_1538del (FLCN)
NM_001353231.2:c.1177-169_1538del (FLCN)