Canonical Allele Identifier: CA1010866459
Gene: CFH HGNC NCBI

Linked Data

dbSNP Id: rs1667988980

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196690532_196690535del , CM000663.2:g.196690532_196690535del GRCh38
NC_000001.10:g.196659662_196659665del , CM000663.1:g.196659662_196659665del GRCh37
NC_000001.9:g.194926285_194926288del NCBI36
NG_007259.1:g.43522_43525del , LRG_47:g.43522_43525del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359637.3:c.1144+293_1144+296del ENSP00000352658.2:n.1144+293_1144+296del
ENST00000470918.2:n.1602+293_1602+296del
ENST00000695968.1:c.1153+293_1153+296del ENSP00000512295.1:n.1153+293_1153+296del
ENST00000695969.1:c.1336+293_1336+296del ENSP00000512296.1:n.1336+293_1336+296del
ENST00000695970.1:c.1336+293_1336+296del ENSP00000512297.1:n.1336+293_1336+296del
ENST00000695971.1:c.1315+293_1315+296del ENSP00000512298.1:n.1315+293_1315+296del
ENST00000695972.1:c.1336+293_1336+296del ENSP00000512299.1:n.1336+293_1336+296del
ENST00000695973.1:c.1336+293_1336+296del ENSP00000512300.1:n.1336+293_1336+296del
ENST00000695974.1:c.1336+293_1336+296del ENSP00000512301.1:n.1336+293_1336+296del
ENST00000695975.1:c.1336+293_1336+296del ENSP00000512302.1:n.1336+293_1336+296del
ENST00000695976.1:c.1147+293_1147+296del ENSP00000512303.1:n.1147+293_1147+296del
ENST00000695977.1:n.177+293_177+296del
ENST00000695978.1:c.1340+289_1340+292del ENSP00000512304.1:n.1340+289_1340+292del
ENST00000695979.1:c.1315+293_1315+296del ENSP00000512305.1:n.1315+293_1315+296del
ENST00000695980.1:n.1456+293_1456+296del
ENST00000695981.1:c.1336+293_1336+296del ENSP00000512306.1:n.1336+293_1336+296del
ENST00000695983.1:c.1336+293_1336+296del ENSP00000512308.1:n.1336+293_1336+296del
ENST00000695984.1:c.244+17369_244+17372del ENSP00000512309.1:n.244+17369_244+17372del
ENST00000695986.1:c.*987+293_*987+296del ENSP00000512311.1:n.*987+293_*987+296del
ENST00000695987.1:c.1147+293_1147+296del ENSP00000512312.1:n.1147+293_1147+296del
ENST00000696018.1:n.1420+293_1420+296del
ENST00000696019.1:n.1420+293_1420+296del
ENST00000696020.1:n.1420+293_1420+296del
ENST00000696021.1:n.1399+293_1399+296del
ENST00000696022.1:n.1424+289_1424+292del
ENST00000696023.1:c.*19+248_*19+251del ENSP00000512334.1:n.*19+248_*19+251del
ENST00000696024.1:n.1420+293_1420+296del
ENST00000696025.1:n.1420+293_1420+296del
ENST00000696026.1:c.1336+293_1336+296del ENSP00000512335.1:n.1336+293_1336+296del
ENST00000696027.1:c.1336+293_1336+296del ENSP00000512336.1:n.1336+293_1336+296del
ENST00000696028.1:c.1336+293_1336+296del ENSP00000512337.1:n.1336+293_1336+296del
ENST00000696029.1:c.1336+293_1336+296del ENSP00000512338.1:n.1336+293_1336+296del
ENST00000696030.1:c.1261+293_1261+296del ENSP00000512339.1:n.1261+293_1261+296del
ENST00000696031.1:c.*854+293_*854+296del ENSP00000512340.1:n.*854+293_*854+296del
ENST00000696032.1:c.1336+293_1336+296del ENSP00000512341.1:n.1336+293_1336+296del
ENST00000696033.1:c.1159+918_1159+921del ENSP00000512342.1:n.1159+918_1159+921del
ENST00000367429.9:c.1336+293_1336+296del MANE Select ENSP00000356399.4:n.1336+293_1336+296del
ENST00000359637.2:c.1144+293_1144+296del ENSP00000352658.2:n.1144+293_1144+296del
ENST00000367429.8:c.1336+293_1336+296del ENSP00000356399.4:n.1336+293_1336+296del
ENST00000466229.5:n.3352+293_3352+296del
ENST00000630130.2:c.1336+293_1336+296del ENSP00000487250.1:n.1336+293_1336+296del
NM_000186.3:c.1336+293_1336+296del , LRG_47t1:c.1336+293_1336+296del NP_000177.2:n.1336+293_1336+296del
NM_001014975.2:c.1336+293_1336+296del NP_001014975.1:n.1336+293_1336+296del
XM_017001108.2:c.1336+293_1336+296del XP_016856597.1:n.1336+293_1336+296del
XR_001737134.2:n.1421+293_1421+296del
NM_000186.4:c.1336+293_1336+296del MANE Select NP_000177.2:n.1336+293_1336+296del
NM_001014975.3:c.1336+293_1336+296del NP_001014975.1:n.1336+293_1336+296del