Canonical Allele Identifier: CA625314087

Gene: FLCN

Linked Data

• dbSNP Id: rs1392167019
• gnomAD v2: 17-17126013-A-ATGGCTTTAAGCCG
• gnomAD v4: 17-17222699-A-ATGGCTTTAAGCCG
• MyVariant Identifiers: chr17:g.17126013_17126014insTGGCTTTAAGCCG (hg19) ; chr17:g.17222699_17222700insTGGCTTTAAGCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17222699_17222700insTGGCTTTAAGCCG , CM000679.2:g.17222699_17222700insTGGCTTTAAGCCG	GRCh38
NC_000017.10:g.17126013_17126014insTGGCTTTAAGCCG , CM000679.1:g.17126013_17126014insTGGCTTTAAGCCG	GRCh37
NC_000017.9:g.17066738_17066739insTGGCTTTAAGCCG	NCBI36
NG_008001.2:g.19489_19490insCGGCTTAAAGCCA , LRG_325:g.19489_19490insCGGCTTAAAGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.619-39_619-38insCGGCTTAAAGCCA MANE Select	ENSP00000285071.4:n.619-39_619-38insCGGCTTAAAGCCA
ENST00000285071.8:c.619-39_619-38insCGGCTTAAAGCCA	ENSP00000285071.4:n.619-39_619-38insCGGCTTAAAGCCA
ENST00000389169.9:c.619-39_619-38insCGGCTTAAAGCCA	ENSP00000373821.5:n.619-39_619-38insCGGCTTAAAGCCA
ENST00000427497.3:c.149-3646_149-3645insCGGCTTAAAGCCA	ENSP00000394249.3:n.149-3646_149-3645insCGGCTTAAAGCCA
ENST00000466317.1:n.423_424insCGGCTTAAAGCCA
ENST00000480316.1:n.585-39_585-38insCGGCTTAAAGCCA
NM_144606.5:c.619-39_619-38insCGGCTTAAAGCCA	NP_653207.1:n.619-39_619-38insCGGCTTAAAGCCA
NM_144997.5:c.619-39_619-38insCGGCTTAAAGCCA , LRG_325t1:c.619-39_619-38insCGGCTTAAAGCCA	NP_659434.2:n.619-39_619-38insCGGCTTAAAGCCA
XM_011523714.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522016.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523715.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522017.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523716.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522018.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523717.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522019.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523718.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522020.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523719.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522021.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523720.1:c.397-39_397-38insCGGCTTAAAGCCA	XP_011522022.1:n.397-39_397-38insCGGCTTAAAGCCA
XM_011523721.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522023.1:n.673-39_673-38insCGGCTTAAAGCCA
XR_934007.1:n.2013-39_2013-38insCGGCTTAAAGCCA
NM_001353229.1:c.673-39_673-38insCGGCTTAAAGCCA	NP_001340158.1:n.673-39_673-38insCGGCTTAAAGCCA
NM_001353230.1:c.619-39_619-38insCGGCTTAAAGCCA	NP_001340159.1:n.619-39_619-38insCGGCTTAAAGCCA
NM_001353231.1:c.619-39_619-38insCGGCTTAAAGCCA	NP_001340160.1:n.619-39_619-38insCGGCTTAAAGCCA
NM_144606.6:c.619-39_619-38insCGGCTTAAAGCCA	NP_653207.1:n.619-39_619-38insCGGCTTAAAGCCA
NM_144997.6:c.619-39_619-38insCGGCTTAAAGCCA	NP_659434.2:n.619-39_619-38insCGGCTTAAAGCCA
XM_011523714.3:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522016.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523718.3:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522020.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523719.3:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522021.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_011523721.3:c.673-39_673-38insCGGCTTAAAGCCA	XP_011522023.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_017024305.2:c.673-39_673-38insCGGCTTAAAGCCA	XP_016879794.1:n.673-39_673-38insCGGCTTAAAGCCA
XM_017024308.1:c.619-39_619-38insCGGCTTAAAGCCA	XP_016879797.1:n.619-39_619-38insCGGCTTAAAGCCA
XM_017024309.2:c.397-39_397-38insCGGCTTAAAGCCA	XP_016879798.1:n.397-39_397-38insCGGCTTAAAGCCA
XM_024450635.1:c.673-39_673-38insCGGCTTAAAGCCA	XP_024306403.1:n.673-39_673-38insCGGCTTAAAGCCA
XR_001752445.2:n.1177-39_1177-38insCGGCTTAAAGCCA
NM_144997.7:c.619-39_619-38insCGGCTTAAAGCCA MANE Select	NP_659434.2:n.619-39_619-38insCGGCTTAAAGCCA
NM_001353229.2:c.673-39_673-38insCGGCTTAAAGCCA	NP_001340158.1:n.673-39_673-38insCGGCTTAAAGCCA
NM_001353230.2:c.619-39_619-38insCGGCTTAAAGCCA	NP_001340159.1:n.619-39_619-38insCGGCTTAAAGCCA
NM_001353231.2:c.619-39_619-38insCGGCTTAAAGCCA	NP_001340160.1:n.619-39_619-38insCGGCTTAAAGCCA
NM_144606.7:c.619-39_619-38insCGGCTTAAAGCCA	NP_653207.1:n.619-39_619-38insCGGCTTAAAGCCA