Canonical Allele Identifier: CA288323923

Gene: FLCN

Linked Data

• dbSNP Id: rs535864585
• gnomAD v3: 17-17231848-T-C
• gnomAD v4: 17-17231848-T-C
• MyVariant Identifiers: chr17:g.17135162T>C (hg19) ; chr17:g.17231848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17231848T>C , CM000679.2:g.17231848T>C	GRCh38
NC_000017.10:g.17135162T>C , CM000679.1:g.17135162T>C	GRCh37
NC_000017.9:g.17075887T>C	NCBI36
NG_008001.2:g.10341A>G , LRG_325:g.10341A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.-79A>G MANE Select	ENSP00000285071.4:n.-79A>G
ENST00000285071.8:c.-79A>G	ENSP00000285071.4:n.-79A>G
ENST00000389169.9:c.-79A>G	ENSP00000373821.5:n.-79A>G
ENST00000389171.4:n.426A>G
ENST00000417064.1:c.-27-3843A>G	ENSP00000410410.1:n.-27-3843A>G
ENST00000427497.3:c.-79A>G	ENSP00000394249.3:n.-79A>G
ENST00000473853.1:n.60A>G
NM_144606.5:c.-79A>G	NP_653207.1:n.-79A>G
NM_144997.5:c.-79A>G , LRG_325t1:c.-79A>G	NP_659434.2:n.-79A>G
XM_011523714.1:c.-79A>G	XP_011522016.1:n.-79A>G
XM_011523715.1:c.-823A>G	XP_011522017.1:n.-823A>G
XM_011523717.1:c.-739A>G	XP_011522019.1:n.-739A>G
XM_011523718.1:c.-25+940A>G	XP_011522020.1:n.-25+940A>G
XM_011523721.1:c.-25+940A>G	XP_011522023.1:n.-25+940A>G
NM_001353229.1:c.-79A>G	NP_001340158.1:n.-79A>G
NM_001353230.1:c.-362A>G	NP_001340159.1:n.-362A>G
NM_001353231.1:c.-278A>G	NP_001340160.1:n.-278A>G
NM_144606.6:c.-79A>G	NP_653207.1:n.-79A>G
NM_144997.6:c.-79A>G	NP_659434.2:n.-79A>G
XM_011523714.3:c.-79A>G	XP_011522016.1:n.-79A>G
XM_011523718.3:c.-25+940A>G	XP_011522020.1:n.-25+940A>G
XM_011523719.3:c.-79A>G	XP_011522021.1:n.-79A>G
XM_011523721.3:c.-25+940A>G	XP_011522023.1:n.-25+940A>G
XM_017024305.2:c.-278A>G	XP_016879794.1:n.-278A>G
XM_017024308.1:c.-278A>G	XP_016879797.1:n.-278A>G
XM_017024309.2:c.-79A>G	XP_016879798.1:n.-79A>G
XM_024450635.1:c.-1287A>G	XP_024306403.1:n.-1287A>G
XR_001752445.2:n.426A>G
NM_144997.7:c.-79A>G MANE Select	NP_659434.2:n.-79A>G
NM_001353229.2:c.-79A>G	NP_001340158.1:n.-79A>G
NM_001353230.2:c.-362A>G	NP_001340159.1:n.-362A>G
NM_001353231.2:c.-278A>G	NP_001340160.1:n.-278A>G
NM_144606.7:c.-79A>G	NP_653207.1:n.-79A>G