Canonical Allele Identifier: CA2250420248

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17227923_17227924delinsCT , CM000679.2:g.17227923_17227924delinsCT	GRCh38
NC_000017.10:g.17131237_17131238delinsCT , CM000679.1:g.17131237_17131238delinsCT	GRCh37
NC_000017.9:g.17071962_17071963delinsCT	NCBI36
NG_008001.2:g.14265_14266delinsAG , LRG_325:g.14265_14266delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285071.9:c.214_215delinsAG MANE Select	ENSP00000285071.4:p.Ser72=
ENST00000285071.8:c.214_215delinsAG	ENSP00000285071.4:p.Ser72=
ENST00000389168.6:n.1554_1555delinsAG
ENST00000389169.9:c.214_215delinsAG	ENSP00000373821.5:p.Ser72=
ENST00000389171.4:n.718_719delinsAG
ENST00000417064.1:c.55_56delinsAG	ENSP00000410410.1:p.Ser19=
ENST00000427497.3:c.148+66_148+67delinsAG	ENSP00000394249.3:n.148+66_148+67delinsAG
NM_144606.5:c.214_215delinsAG	NP_653207.1:p.Ser72=
NM_144997.5:c.214_215delinsAG , LRG_325t1:c.214_215delinsAG	NP_659434.2:p.Ser72=
XM_011523714.1:c.214_215delinsAG	XP_011522016.1:p.Ser72=
XM_011523715.1:c.214_215delinsAG	XP_011522017.1:p.Ser72=
XM_011523716.1:c.214_215delinsAG	XP_011522018.1:p.Ser72=
XM_011523717.1:c.214_215delinsAG	XP_011522019.1:p.Ser72=
XM_011523718.1:c.214_215delinsAG	XP_011522020.1:p.Ser72=
XM_011523719.1:c.214_215delinsAG	XP_011522021.1:p.Ser72=
XM_011523720.1:c.214_215delinsAG	XP_011522022.1:p.Ser72=
XM_011523721.1:c.214_215delinsAG	XP_011522023.1:p.Ser72=
XR_934007.1:n.1554_1555delinsAG
NM_001353229.1:c.214_215delinsAG	NP_001340158.1:p.Ser72=
NM_001353230.1:c.214_215delinsAG	NP_001340159.1:p.Ser72=
NM_001353231.1:c.214_215delinsAG	NP_001340160.1:p.Ser72=
NM_144606.6:c.214_215delinsAG	NP_653207.1:p.Ser72=
NM_144997.6:c.214_215delinsAG	NP_659434.2:p.Ser72=
XM_011523714.3:c.214_215delinsAG	XP_011522016.1:p.Ser72=
XM_011523718.3:c.214_215delinsAG	XP_011522020.1:p.Ser72=
XM_011523719.3:c.214_215delinsAG	XP_011522021.1:p.Ser72=
XM_011523721.3:c.214_215delinsAG	XP_011522023.1:p.Ser72=
XM_017024305.2:c.214_215delinsAG	XP_016879794.1:p.Ser72=
XM_017024308.1:c.214_215delinsAG	XP_016879797.1:p.Ser72=
XM_017024309.2:c.214_215delinsAG	XP_016879798.1:p.Ser72=
XM_024450635.1:c.214_215delinsAG	XP_024306403.1:p.Ser72=
XR_001752445.2:n.718_719delinsAG
NM_144997.7:c.214_215delinsAG MANE Select	NP_659434.2:p.Ser72=
NM_001353229.2:c.214_215delinsAG	NP_001340158.1:p.Ser72=
NM_001353230.2:c.214_215delinsAG	NP_001340159.1:p.Ser72=
NM_001353231.2:c.214_215delinsAG	NP_001340160.1:p.Ser72=
NM_144606.7:c.214_215delinsAG	NP_653207.1:p.Ser72=