Canonical Allele Identifier: CA2501933061

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196690476_196690477insGTAATGT , CM000663.2:g.196690476_196690477insGTAATGT	GRCh38
NC_000001.10:g.196659606_196659607insGTAATGT , CM000663.1:g.196659606_196659607insGTAATGT	GRCh37
NC_000001.9:g.194926229_194926230insGTAATGT	NCBI36
NG_007259.1:g.43466_43467insGTAATGT , LRG_47:g.43466_43467insGTAATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359637.3:c.1144+237_1144+238insGTAATGT	ENSP00000352658.2:n.1144+237_1144+238insGTAATGT
ENST00000470918.2:n.1602+237_1602+238insGTAATGT
ENST00000695968.1:c.1153+237_1153+238insGTAATGT	ENSP00000512295.1:n.1153+237_1153+238insGTAATGT
ENST00000695969.1:c.1336+237_1336+238insGTAATGT	ENSP00000512296.1:n.1336+237_1336+238insGTAATGT
ENST00000695970.1:c.1336+237_1336+238insGTAATGT	ENSP00000512297.1:n.1336+237_1336+238insGTAATGT
ENST00000695971.1:c.1315+237_1315+238insGTAATGT	ENSP00000512298.1:n.1315+237_1315+238insGTAATGT
ENST00000695972.1:c.1336+237_1336+238insGTAATGT	ENSP00000512299.1:n.1336+237_1336+238insGTAATGT
ENST00000695973.1:c.1336+237_1336+238insGTAATGT	ENSP00000512300.1:n.1336+237_1336+238insGTAATGT
ENST00000695974.1:c.1336+237_1336+238insGTAATGT	ENSP00000512301.1:n.1336+237_1336+238insGTAATGT
ENST00000695975.1:c.1336+237_1336+238insGTAATGT	ENSP00000512302.1:n.1336+237_1336+238insGTAATGT
ENST00000695976.1:c.1147+237_1147+238insGTAATGT	ENSP00000512303.1:n.1147+237_1147+238insGTAATGT
ENST00000695977.1:n.177+237_177+238insGTAATGT
ENST00000695978.1:c.1340+233_1340+234insGTAATGT	ENSP00000512304.1:n.1340+233_1340+234insGTAATGT
ENST00000695979.1:c.1315+237_1315+238insGTAATGT	ENSP00000512305.1:n.1315+237_1315+238insGTAATGT
ENST00000695980.1:n.1456+237_1456+238insGTAATGT
ENST00000695981.1:c.1336+237_1336+238insGTAATGT	ENSP00000512306.1:n.1336+237_1336+238insGTAATGT
ENST00000695983.1:c.1336+237_1336+238insGTAATGT	ENSP00000512308.1:n.1336+237_1336+238insGTAATGT
ENST00000695984.1:c.244+17313_244+17314insGTAATGT	ENSP00000512309.1:n.244+17313_244+17314insGTAATGT
ENST00000695986.1:c.*987+237_*987+238insGTAATGT	ENSP00000512311.1:n.*987+237_*987+238insGTAATGT
ENST00000695987.1:c.1147+237_1147+238insGTAATGT	ENSP00000512312.1:n.1147+237_1147+238insGTAATGT
ENST00000696018.1:n.1420+237_1420+238insGTAATGT
ENST00000696019.1:n.1420+237_1420+238insGTAATGT
ENST00000696020.1:n.1420+237_1420+238insGTAATGT
ENST00000696021.1:n.1399+237_1399+238insGTAATGT
ENST00000696022.1:n.1424+233_1424+234insGTAATGT
ENST00000696023.1:c.*19+192_*19+193insGTAATGT	ENSP00000512334.1:n.*19+192_*19+193insGTAATGT
ENST00000696024.1:n.1420+237_1420+238insGTAATGT
ENST00000696025.1:n.1420+237_1420+238insGTAATGT
ENST00000696026.1:c.1336+237_1336+238insGTAATGT	ENSP00000512335.1:n.1336+237_1336+238insGTAATGT
ENST00000696027.1:c.1336+237_1336+238insGTAATGT	ENSP00000512336.1:n.1336+237_1336+238insGTAATGT
ENST00000696028.1:c.1336+237_1336+238insGTAATGT	ENSP00000512337.1:n.1336+237_1336+238insGTAATGT
ENST00000696029.1:c.1336+237_1336+238insGTAATGT	ENSP00000512338.1:n.1336+237_1336+238insGTAATGT
ENST00000696030.1:c.1261+237_1261+238insGTAATGT	ENSP00000512339.1:n.1261+237_1261+238insGTAATGT
ENST00000696031.1:c.*854+237_*854+238insGTAATGT	ENSP00000512340.1:n.*854+237_*854+238insGTAATGT
ENST00000696032.1:c.1336+237_1336+238insGTAATGT	ENSP00000512341.1:n.1336+237_1336+238insGTAATGT
ENST00000696033.1:c.1159+862_1159+863insGTAATGT	ENSP00000512342.1:n.1159+862_1159+863insGTAATGT
ENST00000367429.9:c.1336+237_1336+238insGTAATGT MANE Select	ENSP00000356399.4:n.1336+237_1336+238insGTAATGT
ENST00000359637.2:c.1144+237_1144+238insGTAATGT	ENSP00000352658.2:n.1144+237_1144+238insGTAATGT
ENST00000367429.8:c.1336+237_1336+238insGTAATGT	ENSP00000356399.4:n.1336+237_1336+238insGTAATGT
ENST00000466229.5:n.3352+237_3352+238insGTAATGT
ENST00000630130.2:c.1336+237_1336+238insGTAATGT	ENSP00000487250.1:n.1336+237_1336+238insGTAATGT
NM_000186.3:c.1336+237_1336+238insGTAATGT , LRG_47t1:c.1336+237_1336+238insGTAATGT	NP_000177.2:n.1336+237_1336+238insGTAATGT
NM_001014975.2:c.1336+237_1336+238insGTAATGT	NP_001014975.1:n.1336+237_1336+238insGTAATGT
XM_017001108.2:c.1336+237_1336+238insGTAATGT	XP_016856597.1:n.1336+237_1336+238insGTAATGT
XR_001737134.2:n.1421+237_1421+238insGTAATGT
NM_000186.4:c.1336+237_1336+238insGTAATGT MANE Select	NP_000177.2:n.1336+237_1336+238insGTAATGT
NM_001014975.3:c.1336+237_1336+238insGTAATGT	NP_001014975.1:n.1336+237_1336+238insGTAATGT