Canonical Allele Identifier: CA1217753859

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196710267_196710268delinsCT , CM000663.2:g.196710267_196710268delinsCT	GRCh38
NC_000001.10:g.196679397_196679398delinsCT , CM000663.1:g.196679397_196679398delinsCT	GRCh37
NC_000001.9:g.194946020_194946021delinsCT	NCBI36
NG_007259.1:g.63257_63258delinsCT , LRG_47:g.63257_63258delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.1603-3468_1603-3467delinsCT
ENST00000695969.1:c.1337-3468_1337-3467delinsCT	ENSP00000512296.1:n.1337-3468_1337-3467de...
ENST00000695970.1:c.1337-3468_1337-3467delinsCT	ENSP00000512297.1:n.1337-3468_1337-3467de...
ENST00000695971.1:c.1316-3468_1316-3467delinsCT	ENSP00000512298.1:n.1316-3468_1316-3467de...
ENST00000695972.1:c.1337-3468_1337-3467delinsCT	ENSP00000512299.1:n.1337-3468_1337-3467de...
ENST00000695973.1:c.1337-3468_1337-3467delinsCT	ENSP00000512300.1:n.1337-3468_1337-3467de...
ENST00000695974.1:c.1337-3468_1337-3467delinsCT	ENSP00000512301.1:n.1337-3468_1337-3467de...
ENST00000695975.1:c.1337-3468_1337-3467delinsCT	ENSP00000512302.1:n.1337-3468_1337-3467de...
ENST00000695976.1:c.1148-3468_1148-3467delinsCT	ENSP00000512303.1:n.1148-3468_1148-3467de...
ENST00000695981.1:c.1337-3468_1337-3467delinsCT	ENSP00000512306.1:n.1337-3468_1337-3467de...
ENST00000695983.1:c.1337-3468_1337-3467delinsCT	ENSP00000512308.1:n.1337-3468_1337-3467de...
ENST00000695984.1:c.245-18079_245-18078delinsCT	ENSP00000512309.1:n.245-18079_245-18078de...
ENST00000695986.1:c.*988-3468_*988-3467delinsCT	ENSP00000512311.1:n.*988-3468_*988-3467de...
ENST00000696024.1:n.1421-3468_1421-3467delinsCT
ENST00000696025.1:n.1421-3468_1421-3467delinsCT
ENST00000696026.1:c.1337-3468_1337-3467delinsCT	ENSP00000512335.1:n.1337-3468_1337-3467de...
ENST00000696027.1:c.1337-3468_1337-3467delinsCT	ENSP00000512336.1:n.1337-3468_1337-3467de...
ENST00000696028.1:c.1337-3468_1337-3467delinsCT	ENSP00000512337.1:n.1337-3468_1337-3467de...
ENST00000696029.1:c.1337-3468_1337-3467delinsCT	ENSP00000512338.1:n.1337-3468_1337-3467de...
ENST00000696031.1:c.*855-3468_*855-3467delinsCT	ENSP00000512340.1:n.*855-3468_*855-3467de...
ENST00000696032.1:c.1337-3468_1337-3467delinsCT	ENSP00000512341.1:n.1337-3468_1337-3467de...
ENST00000696033.1:c.1159+20653_1159+20654delinsCT	ENSP00000512342.1:n.1159+20653_1159+20654...
ENST00000367429.9:c.1337-3468_1337-3467delinsCT MANE Select	ENSP00000356399.4:n.1337-3468_1337-3467de...
ENST00000367429.8:c.1337-3468_1337-3467delinsCT	ENSP00000356399.4:n.1337-3468_1337-3467de...
ENST00000466229.5:n.3353-3468_3353-3467delinsCT
NM_000186.3:c.1337-3468_1337-3467delinsCT , LRG_47t1:c.1337-3468_1337-3467delinsCT	NP_000177.2:n.1337-3468_1337-3467delinsCT...
XR_001737134.2:n.1422-3468_1422-3467delinsCT
NM_000186.4:c.1337-3468_1337-3467delinsCT MANE Select	NP_000177.2:n.1337-3468_1337-3467delinsCT...