Canonical Allele Identifier: CA1217743321

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196690165C= , CM000663.2:g.196690165C=	GRCh38
NC_000001.10:g.196659295C= , CM000663.1:g.196659295C=	GRCh37
NC_000001.9:g.194925918C=	NCBI36
NG_007259.1:g.43155C= , LRG_47:g.43155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359637.3:c.1070C=	ENSP00000352658.2:p.Ala357=
ENST00000470918.2:n.1528C=
ENST00000695968.1:c.1079C=	ENSP00000512295.1:p.Ala360=
ENST00000695969.1:c.1262C=	ENSP00000512296.1:p.Ala421=
ENST00000695970.1:c.1262C=	ENSP00000512297.1:p.Ala421=
ENST00000695971.1:c.1241C=	ENSP00000512298.1:p.Ala414=
ENST00000695972.1:c.1262C=	ENSP00000512299.1:p.Ala421=
ENST00000695973.1:c.1262C=	ENSP00000512300.1:p.Ala421=
ENST00000695974.1:c.1262C=	ENSP00000512301.1:p.Ala421=
ENST00000695975.1:c.1262C=	ENSP00000512302.1:p.Ala421=
ENST00000695976.1:c.1073C=	ENSP00000512303.1:p.Ala358=
ENST00000695977.1:n.103C=
ENST00000695978.1:c.1262C=	ENSP00000512304.1:p.Ala421=
ENST00000695979.1:c.1241C=	ENSP00000512305.1:p.Ala414=
ENST00000695980.1:n.1382C=
ENST00000695981.1:c.1262C=	ENSP00000512306.1:p.Ala421=
ENST00000695983.1:c.1262C=	ENSP00000512308.1:p.Ala421=
ENST00000695984.1:c.244+17002C=	ENSP00000512309.1:n.244+17002C=
ENST00000695986.1:c.*913C=	ENSP00000512311.1:n.*913C=
ENST00000695987.1:c.1073C=	ENSP00000512312.1:p.Ala358=
ENST00000696018.1:n.1346C=
ENST00000696019.1:n.1346C=
ENST00000696020.1:n.1346C=
ENST00000696021.1:n.1325C=
ENST00000696022.1:n.1346C=
ENST00000696023.1:c.1262C=	ENSP00000512334.1:p.Ala421=
ENST00000696024.1:n.1346C=
ENST00000696025.1:n.1346C=
ENST00000696026.1:c.1262C=	ENSP00000512335.1:p.Ala421=
ENST00000696027.1:c.1262C=	ENSP00000512336.1:p.Ala421=
ENST00000696028.1:c.1262C=	ENSP00000512337.1:p.Ala421=
ENST00000696029.1:c.1262C=	ENSP00000512338.1:p.Ala421=
ENST00000696030.1:c.1187C=	ENSP00000512339.1:p.Ala396=
ENST00000696031.1:c.*780C=	ENSP00000512340.1:n.*780C=
ENST00000696032.1:c.1262C=	ENSP00000512341.1:p.Ala421=
ENST00000696033.1:c.1159+551C=	ENSP00000512342.1:n.1159+551C=
ENST00000367429.9:c.1262C= MANE Select	ENSP00000356399.4:p.Ala421=
ENST00000359637.2:c.1070C=	ENSP00000352658.2:p.Ala357=
ENST00000367429.8:c.1262C=	ENSP00000356399.4:p.Ala421=
ENST00000466229.5:n.3278C=
ENST00000630130.2:c.1262C=	ENSP00000487250.1:p.Ala421=
NM_000186.3:c.1262C= , LRG_47t1:c.1262C=	NP_000177.2:p.Ala421=
NM_001014975.2:c.1262C=	NP_001014975.1:p.Ala421=
XM_017001108.2:c.1262C=	XP_016856597.1:p.Ala421=
XR_001737134.2:n.1347C=
NM_000186.4:c.1262C= MANE Select	NP_000177.2:p.Ala421=
NM_001014975.3:c.1262C=	NP_001014975.1:p.Ala421=