Canonical Allele Identifier: CA1217770847

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747427A= , CM000663.2:g.196747427A=	GRCh38
NC_000001.10:g.196716557A= , CM000663.1:g.196716557A=	GRCh37
NC_000001.9:g.194983180A=	NCBI36
NG_007259.1:g.100417A= , LRG_47:g.100417A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4838A=
ENST00000695970.1:c.*114A=	ENSP00000512297.1:n.*114A=
ENST00000695971.1:c.*114A=	ENSP00000512298.1:n.*114A=
ENST00000695972.1:c.*887A=	ENSP00000512299.1:n.*887A=
ENST00000695973.1:c.*2174A=	ENSP00000512300.1:n.*2174A=
ENST00000695974.1:c.*114A=	ENSP00000512301.1:n.*114A=
ENST00000695975.1:c.*1937A=	ENSP00000512302.1:n.*1937A=
ENST00000695976.1:c.*114A=	ENSP00000512303.1:n.*114A=
ENST00000695981.1:c.3580+230A=	ENSP00000512306.1:n.3580+230A=
ENST00000695984.1:c.*114A=	ENSP00000512309.1:n.*114A=
ENST00000695986.1:c.*3461A=	ENSP00000512311.1:n.*3461A=
ENST00000695990.1:n.844A=
ENST00000696026.1:c.*2092A=	ENSP00000512335.1:n.*2092A=
ENST00000696027.1:c.*114A=	ENSP00000512336.1:n.*114A=
ENST00000696028.1:c.*114A=	ENSP00000512337.1:n.*114A=
ENST00000696029.1:c.*114A=	ENSP00000512338.1:n.*114A=
ENST00000696031.1:c.*3328A=	ENSP00000512340.1:n.*3328A=
ENST00000696032.1:c.3580+230A=	ENSP00000512341.1:n.3580+230A=
ENST00000696033.1:c.1160-32370A=	ENSP00000512342.1:n.1160-32370A=
ENST00000367429.9:c.*114A= MANE Select	ENSP00000356399.4:n.*114A=
ENST00000367429.8:c.*114A=	ENSP00000356399.4:n.*114A=
ENST00000466229.5:n.6908A=
NM_000186.3:c.*114A= , LRG_47t1:c.*114A=	NP_000177.2:n.*114A=
XR_001737134.2:n.3996A=
NM_000186.4:c.*114A= MANE Select	NP_000177.2:n.*114A=