Canonical Allele Identifier: CA1217768973

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743477A= , CM000663.2:g.196743477A=	GRCh38
NC_000001.10:g.196712607A= , CM000663.1:g.196712607A=	GRCh37
NC_000001.9:g.194979230A=	NCBI36
NG_007259.1:g.96467A= , LRG_47:g.96467A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4187A=
ENST00000695970.1:c.2985A=	ENSP00000512297.1:p.Thr995=
ENST00000695971.1:c.3138A=	ENSP00000512298.1:p.Thr1046=
ENST00000695972.1:c.*236A=	ENSP00000512299.1:n.*236A=
ENST00000695973.1:c.*1523A=	ENSP00000512300.1:n.*1523A=
ENST00000695974.1:c.2982A=	ENSP00000512301.1:p.Thr994=
ENST00000695975.1:c.*1286A=	ENSP00000512302.1:n.*1286A=
ENST00000695976.1:c.2970A=	ENSP00000512303.1:p.Thr990=
ENST00000695981.1:c.3159A=	ENSP00000512306.1:p.Thr1053=
ENST00000695984.1:c.1167A=	ENSP00000512309.1:p.Thr389=
ENST00000695986.1:c.*2810A=	ENSP00000512311.1:n.*2810A=
ENST00000696026.1:c.*1441A=	ENSP00000512335.1:n.*1441A=
ENST00000696027.1:c.3153A=	ENSP00000512336.1:p.Thr1051=
ENST00000696028.1:c.3087A=	ENSP00000512337.1:p.Thr1029=
ENST00000696029.1:c.3153A=	ENSP00000512338.1:p.Thr1051=
ENST00000696031.1:c.*2677A=	ENSP00000512340.1:n.*2677A=
ENST00000696032.1:c.3159A=	ENSP00000512341.1:p.Thr1053=
ENST00000696033.1:c.1160-36320A=	ENSP00000512342.1:n.1160-36320A=
ENST00000367429.9:c.3159A= MANE Select	ENSP00000356399.4:p.Thr1053=
ENST00000367429.8:c.3159A=	ENSP00000356399.4:p.Thr1053=
ENST00000466229.5:n.6257A=
NM_000186.3:c.3159A= , LRG_47t1:c.3159A=	NP_000177.2:p.Thr1053=
XR_001737134.2:n.3345A=
NM_000186.4:c.3159A= MANE Select	NP_000177.2:p.Thr1053=