Canonical Allele Identifier: CA1217746008
Gene: CFH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196694700C= , CM000663.2:g.196694700C= GRCh38
NC_000001.10:g.196663830C= , CM000663.1:g.196663830C= GRCh37
NC_000001.9:g.194930453C= NCBI36
NG_007259.1:g.47690C= , LRG_47:g.47690C=

Transcript Alleles

HGVS Amino-acid change
ENST00000359637.3:c.1144+4461C= ENSP00000352658.2:n.1144+4461C=
ENST00000470918.2:n.1602+4461C=
ENST00000695968.1:c.1153+4461C= ENSP00000512295.1:n.1153+4461C=
ENST00000695969.1:c.1336+4461C= ENSP00000512296.1:n.1336+4461C=
ENST00000695970.1:c.1336+4461C= ENSP00000512297.1:n.1336+4461C=
ENST00000695971.1:c.1315+4461C= ENSP00000512298.1:n.1315+4461C=
ENST00000695972.1:c.1336+4461C= ENSP00000512299.1:n.1336+4461C=
ENST00000695973.1:c.1336+4461C= ENSP00000512300.1:n.1336+4461C=
ENST00000695974.1:c.1336+4461C= ENSP00000512301.1:n.1336+4461C=
ENST00000695975.1:c.1336+4461C= ENSP00000512302.1:n.1336+4461C=
ENST00000695976.1:c.1147+4461C= ENSP00000512303.1:n.1147+4461C=
ENST00000695978.1:c.1340+4457C= ENSP00000512304.1:n.1340+4457C=
ENST00000695979.1:c.1315+4461C= ENSP00000512305.1:n.1315+4461C=
ENST00000695980.1:n.1456+4461C=
ENST00000695981.1:c.1336+4461C= ENSP00000512306.1:n.1336+4461C=
ENST00000695983.1:c.1336+4461C= ENSP00000512308.1:n.1336+4461C=
ENST00000695984.1:c.244+21537C= ENSP00000512309.1:n.244+21537C=
ENST00000695986.1:c.*987+4461C= ENSP00000512311.1:n.*987+4461C=
ENST00000695987.1:c.1147+4461C= ENSP00000512312.1:n.1147+4461C=
ENST00000696018.1:n.1421-1350C=
ENST00000696019.1:n.1420+4461C=
ENST00000696020.1:n.1420+4461C=
ENST00000696021.1:n.1399+4461C=
ENST00000696022.1:n.1424+4457C=
ENST00000696023.1:c.*19+4416C= ENSP00000512334.1:n.*19+4416C=
ENST00000696024.1:n.1420+4461C=
ENST00000696025.1:n.1420+4461C=
ENST00000696026.1:c.1336+4461C= ENSP00000512335.1:n.1336+4461C=
ENST00000696027.1:c.1336+4461C= ENSP00000512336.1:n.1336+4461C=
ENST00000696028.1:c.1336+4461C= ENSP00000512337.1:n.1336+4461C=
ENST00000696029.1:c.1336+4461C= ENSP00000512338.1:n.1336+4461C=
ENST00000696030.1:c.1261+4461C= ENSP00000512339.1:n.1261+4461C=
ENST00000696031.1:c.*854+4461C= ENSP00000512340.1:n.*854+4461C=
ENST00000696032.1:c.1336+4461C= ENSP00000512341.1:n.1336+4461C=
ENST00000696033.1:c.1159+5086C= ENSP00000512342.1:n.1159+5086C=
ENST00000367429.9:c.1336+4461C= MANE Select ENSP00000356399.4:n.1336+4461C=
ENST00000359637.2:c.1144+4461C= ENSP00000352658.2:n.1144+4461C=
ENST00000367429.8:c.1336+4461C= ENSP00000356399.4:n.1336+4461C=
ENST00000466229.5:n.3352+4461C=
ENST00000630130.2:c.1336+4461C= ENSP00000487250.1:n.1336+4461C=
NM_000186.3:c.1336+4461C= , LRG_47t1:c.1336+4461C= NP_000177.2:n.1336+4461C=
NM_001014975.2:c.1336+4461C= NP_001014975.1:n.1336+4461C=
XR_001737134.2:n.1421+4461C=
NM_000186.4:c.1336+4461C= MANE Select NP_000177.2:n.1336+4461C=
NM_001014975.3:c.1336+4461C= NP_001014975.1:n.1336+4461C=