Canonical Allele Identifier: CA2695224454

Gene: FLCN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17224085_17224101del , CM000679.2:g.17224085_17224101del	GRCh38
NC_000017.10:g.17127399_17127415del , CM000679.1:g.17127399_17127415del	GRCh37
NC_000017.9:g.17068124_17068140del	NCBI36
NG_008001.2:g.18092_18108del , LRG_325:g.18092_18108del

Transcript Alleles

HGVS	Amino-acid change
ENST00000285071.9:c.443_459del MANE Select	ENSP00000285071.4:p.His148ProfsTer?
ENST00000285071.8:c.443_459del	ENSP00000285071.4:p.His148ProfsTer?
ENST00000389169.9:c.443_459del	ENSP00000373821.5:p.His148ProfsTer?
ENST00000417064.1:c.284_300del	ENSP00000410410.1:p.His95ProfsTer?
ENST00000427497.3:c.148+3893_148+3909del	ENSP00000394249.3:n.148+3893_148+3909del
ENST00000480316.1:n.409_425del
NM_144606.5:c.443_459del	NP_653207.1:p.His148ProfsTer?
NM_144997.5:c.443_459del , LRG_325t1:c.443_459del	NP_659434.2:p.His148ProfsTer?
XM_011523714.1:c.497_513del	XP_011522016.1:p.His166ProfsTer?
XM_011523715.1:c.497_513del	XP_011522017.1:p.His166ProfsTer?
XM_011523716.1:c.497_513del	XP_011522018.1:p.His166ProfsTer?
XM_011523717.1:c.497_513del	XP_011522019.1:p.His166ProfsTer?
XM_011523718.1:c.497_513del	XP_011522020.1:p.His166ProfsTer?
XM_011523719.1:c.497_513del	XP_011522021.1:p.His166ProfsTer?
XM_011523720.1:c.397-1436_397-1420del	XP_011522022.1:n.397-1436_397-1420del
XM_011523721.1:c.497_513del	XP_011522023.1:p.His166ProfsTer?
XR_934007.1:n.1837_1853del
NM_001353229.1:c.497_513del	NP_001340158.1:p.His166ProfsTer?
NM_001353230.1:c.443_459del	NP_001340159.1:p.His148ProfsTer?
NM_001353231.1:c.443_459del	NP_001340160.1:p.His148ProfsTer?
NM_144606.6:c.443_459del	NP_653207.1:p.His148ProfsTer?
NM_144997.6:c.443_459del	NP_659434.2:p.His148ProfsTer?
XM_011523714.3:c.497_513del	XP_011522016.1:p.His166ProfsTer?
XM_011523718.3:c.497_513del	XP_011522020.1:p.His166ProfsTer?
XM_011523719.3:c.497_513del	XP_011522021.1:p.His166ProfsTer?
XM_011523721.3:c.497_513del	XP_011522023.1:p.His166ProfsTer?
XM_017024305.2:c.497_513del	XP_016879794.1:p.His166ProfsTer?
XM_017024308.1:c.443_459del	XP_016879797.1:p.His148ProfsTer?
XM_017024309.2:c.397-1436_397-1420del	XP_016879798.1:n.397-1436_397-1420del
XM_024450635.1:c.497_513del	XP_024306403.1:p.His166ProfsTer?
XR_001752445.2:n.1001_1017del
NM_144997.7:c.443_459del MANE Select	NP_659434.2:p.His148ProfsTer?
NM_001353229.2:c.497_513del	NP_001340158.1:p.His166ProfsTer?
NM_001353230.2:c.443_459del	NP_001340159.1:p.His148ProfsTer?
NM_001353231.2:c.443_459del	NP_001340160.1:p.His148ProfsTer?
NM_144606.7:c.443_459del	NP_653207.1:p.His148ProfsTer?