Canonical Allele Identifier: CA1217769032

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743598G= , CM000663.2:g.196743598G=	GRCh38
NC_000001.10:g.196712728G= , CM000663.1:g.196712728G=	GRCh37
NC_000001.9:g.194979351G=	NCBI36
NG_007259.1:g.96588G= , LRG_47:g.96588G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4308G=
ENST00000695970.1:c.3106G=	ENSP00000512297.1:p.Gly1036=
ENST00000695971.1:c.3259G=	ENSP00000512298.1:p.Gly1087=
ENST00000695972.1:c.*357G=	ENSP00000512299.1:n.*357G=
ENST00000695973.1:c.*1644G=	ENSP00000512300.1:n.*1644G=
ENST00000695974.1:c.3103G=	ENSP00000512301.1:p.Gly1035=
ENST00000695975.1:c.*1407G=	ENSP00000512302.1:n.*1407G=
ENST00000695976.1:c.3091G=	ENSP00000512303.1:p.Gly1031=
ENST00000695981.1:c.3280G=	ENSP00000512306.1:p.Gly1094=
ENST00000695984.1:c.1288G=	ENSP00000512309.1:p.Gly430=
ENST00000695986.1:c.*2931G=	ENSP00000512311.1:n.*2931G=
ENST00000696026.1:c.*1562G=	ENSP00000512335.1:n.*1562G=
ENST00000696027.1:c.3274G=	ENSP00000512336.1:p.Gly1092=
ENST00000696028.1:c.3208G=	ENSP00000512337.1:p.Gly1070=
ENST00000696029.1:c.3274G=	ENSP00000512338.1:p.Gly1092=
ENST00000696031.1:c.*2798G=	ENSP00000512340.1:n.*2798G=
ENST00000696032.1:c.3280G=	ENSP00000512341.1:p.Gly1094=
ENST00000696033.1:c.1160-36199G=	ENSP00000512342.1:n.1160-36199G=
ENST00000367429.9:c.3280G= MANE Select	ENSP00000356399.4:p.Gly1094=
ENST00000367429.8:c.3280G=	ENSP00000356399.4:p.Gly1094=
ENST00000466229.5:n.6378G=
NM_000186.3:c.3280G= , LRG_47t1:c.3280G=	NP_000177.2:p.Gly1094=
XR_001737134.2:n.3466G=
NM_000186.4:c.3280G= MANE Select	NP_000177.2:p.Gly1094=