Canonical Allele Identifier: CA2573628165

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196704713_196704714insTC , CM000663.2:g.196704713_196704714insTC	GRCh38
NC_000001.10:g.196673843_196673844insTC , CM000663.1:g.196673843_196673844insTC	GRCh37
NC_000001.9:g.194940466_194940467insTC	NCBI36
NG_007259.1:g.57703_57704insTC , LRG_47:g.57703_57704insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.1603-9022_1603-9021insTC
ENST00000695969.1:c.1337-9022_1337-9021insTC	ENSP00000512296.1:n.1337-9022_1337-9021insTC
ENST00000695970.1:c.1337-9022_1337-9021insTC	ENSP00000512297.1:n.1337-9022_1337-9021insTC
ENST00000695971.1:c.1316-9022_1316-9021insTC	ENSP00000512298.1:n.1316-9022_1316-9021insTC
ENST00000695972.1:c.1337-9022_1337-9021insTC	ENSP00000512299.1:n.1337-9022_1337-9021insTC
ENST00000695973.1:c.1337-9022_1337-9021insTC	ENSP00000512300.1:n.1337-9022_1337-9021insTC
ENST00000695974.1:c.1337-9022_1337-9021insTC	ENSP00000512301.1:n.1337-9022_1337-9021insTC
ENST00000695975.1:c.1337-9022_1337-9021insTC	ENSP00000512302.1:n.1337-9022_1337-9021insTC
ENST00000695976.1:c.1148-9022_1148-9021insTC	ENSP00000512303.1:n.1148-9022_1148-9021insTC
ENST00000695980.1:n.1457-1265_1457-1264insTC
ENST00000695981.1:c.1337-9022_1337-9021insTC	ENSP00000512306.1:n.1337-9022_1337-9021insTC
ENST00000695983.1:c.1337-9022_1337-9021insTC	ENSP00000512308.1:n.1337-9022_1337-9021insTC
ENST00000695984.1:c.245-23633_245-23632insTC	ENSP00000512309.1:n.245-23633_245-23632insTC
ENST00000695986.1:c.*988-9022_*988-9021insTC	ENSP00000512311.1:n.*988-9022_*988-9021insTC
ENST00000696024.1:n.1421-9022_1421-9021insTC
ENST00000696025.1:n.1421-9022_1421-9021insTC
ENST00000696026.1:c.1337-9022_1337-9021insTC	ENSP00000512335.1:n.1337-9022_1337-9021insTC
ENST00000696027.1:c.1337-9022_1337-9021insTC	ENSP00000512336.1:n.1337-9022_1337-9021insTC
ENST00000696028.1:c.1337-9022_1337-9021insTC	ENSP00000512337.1:n.1337-9022_1337-9021insTC
ENST00000696029.1:c.1337-9022_1337-9021insTC	ENSP00000512338.1:n.1337-9022_1337-9021insTC
ENST00000696031.1:c.*855-9022_*855-9021insTC	ENSP00000512340.1:n.*855-9022_*855-9021insTC
ENST00000696032.1:c.1337-9022_1337-9021insTC	ENSP00000512341.1:n.1337-9022_1337-9021insTC
ENST00000696033.1:c.1159+15099_1159+15100insTC	ENSP00000512342.1:n.1159+15099_1159+15100insTC
ENST00000367429.9:c.1337-9022_1337-9021insTC MANE Select	ENSP00000356399.4:n.1337-9022_1337-9021insTC
ENST00000367429.8:c.1337-9022_1337-9021insTC	ENSP00000356399.4:n.1337-9022_1337-9021insTC
ENST00000466229.5:n.3353-9022_3353-9021insTC
NM_000186.3:c.1337-9022_1337-9021insTC , LRG_47t1:c.1337-9022_1337-9021insTC	NP_000177.2:n.1337-9022_1337-9021insTC
XR_001737134.2:n.1422-9022_1422-9021insTC
NM_000186.4:c.1337-9022_1337-9021insTC MANE Select	NP_000177.2:n.1337-9022_1337-9021insTC