Canonical Allele Identifier: CA1217764921
Gene: CFH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196734588_196734589delinsCT , CM000663.2:g.196734588_196734589delinsCT GRCh38
NC_000001.10:g.196703718_196703719delinsCT , CM000663.1:g.196703718_196703719delinsCT GRCh37
NC_000001.9:g.194970341_194970342delinsCT NCBI36
NG_007259.1:g.87578_87579delinsCT , LRG_47:g.87578_87579delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000470918.2:n.2680-2236_2680-2235delinsCT
ENST00000695969.1:c.2414-2236_2414-2235delinsCT ENSP00000512296.1:n.2414-2236_2414-2235de...
ENST00000695970.1:c.2414-2236_2414-2235delinsCT ENSP00000512297.1:n.2414-2236_2414-2235de...
ENST00000695971.1:c.2393-2236_2393-2235delinsCT ENSP00000512298.1:n.2393-2236_2393-2235de...
ENST00000695972.1:c.2233-6076_2233-6075delinsCT ENSP00000512299.1:n.2233-6076_2233-6075de...
ENST00000695973.1:c.*778-2236_*778-2235delinsCT ENSP00000512300.1:n.*778-2236_*778-2235de...
ENST00000695974.1:c.2237-2236_2237-2235delinsCT ENSP00000512301.1:n.2237-2236_2237-2235de...
ENST00000695975.1:c.*541-2236_*541-2235delinsCT ENSP00000512302.1:n.*541-2236_*541-2235de...
ENST00000695976.1:c.2225-2236_2225-2235delinsCT ENSP00000512303.1:n.2225-2236_2225-2235de...
ENST00000695981.1:c.2414-2236_2414-2235delinsCT ENSP00000512306.1:n.2414-2236_2414-2235de...
ENST00000695983.1:c.2414-2236_2414-2235delinsCT ENSP00000512308.1:n.2414-2236_2414-2235de...
ENST00000695984.1:c.422-2236_422-2235delinsCT ENSP00000512309.1:n.422-2236_422-2235deli...
ENST00000695986.1:c.*2065-2236_*2065-2235delinsCT ENSP00000512311.1:n.*2065-2236_*2065-2235...
ENST00000696025.1:n.2498-2236_2498-2235delinsCT
ENST00000696026.1:c.*696-2236_*696-2235delinsCT ENSP00000512335.1:n.*696-2236_*696-2235de...
ENST00000696027.1:c.2408-2236_2408-2235delinsCT ENSP00000512336.1:n.2408-2236_2408-2235de...
ENST00000696028.1:c.2414-2236_2414-2235delinsCT ENSP00000512337.1:n.2414-2236_2414-2235de...
ENST00000696029.1:c.2414-2236_2414-2235delinsCT ENSP00000512338.1:n.2414-2236_2414-2235de...
ENST00000696031.1:c.*1932-2236_*1932-2235delinsCT ENSP00000512340.1:n.*1932-2236_*1932-2235...
ENST00000696032.1:c.2414-2236_2414-2235delinsCT ENSP00000512341.1:n.2414-2236_2414-2235de...
ENST00000696033.1:c.1159+44974_1159+44975delinsCT ENSP00000512342.1:n.1159+44974_1159+44975...
ENST00000367429.9:c.2414-2236_2414-2235delinsCT MANE Select ENSP00000356399.4:n.2414-2236_2414-2235de...
ENST00000367429.8:c.2414-2236_2414-2235delinsCT ENSP00000356399.4:n.2414-2236_2414-2235de...
ENST00000466229.5:n.4430-2236_4430-2235delinsCT
NM_000186.3:c.2414-2236_2414-2235delinsCT , LRG_47t1:c.2414-2236_2414-2235delinsCT NP_000177.2:n.2414-2236_2414-2235delinsCT...
XR_001737134.2:n.2600-2236_2600-2235delinsCT
NM_000186.4:c.2414-2236_2414-2235delinsCT MANE Select NP_000177.2:n.2414-2236_2414-2235delinsCT...