Canonical Allele Identifier: CA1217769009

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743547T= , CM000663.2:g.196743547T=	GRCh38
NC_000001.10:g.196712677T= , CM000663.1:g.196712677T=	GRCh37
NC_000001.9:g.194979300T=	NCBI36
NG_007259.1:g.96537T= , LRG_47:g.96537T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4257T=
ENST00000695970.1:c.3055T=	ENSP00000512297.1:p.Cys1019=
ENST00000695971.1:c.3208T=	ENSP00000512298.1:p.Cys1070=
ENST00000695972.1:c.*306T=	ENSP00000512299.1:n.*306T=
ENST00000695973.1:c.*1593T=	ENSP00000512300.1:n.*1593T=
ENST00000695974.1:c.3052T=	ENSP00000512301.1:p.Cys1018=
ENST00000695975.1:c.*1356T=	ENSP00000512302.1:n.*1356T=
ENST00000695976.1:c.3040T=	ENSP00000512303.1:p.Cys1014=
ENST00000695981.1:c.3229T=	ENSP00000512306.1:p.Cys1077=
ENST00000695984.1:c.1237T=	ENSP00000512309.1:p.Cys413=
ENST00000695986.1:c.*2880T=	ENSP00000512311.1:n.*2880T=
ENST00000696026.1:c.*1511T=	ENSP00000512335.1:n.*1511T=
ENST00000696027.1:c.3223T=	ENSP00000512336.1:p.Cys1075=
ENST00000696028.1:c.3157T=	ENSP00000512337.1:p.Cys1053=
ENST00000696029.1:c.3223T=	ENSP00000512338.1:p.Cys1075=
ENST00000696031.1:c.*2747T=	ENSP00000512340.1:n.*2747T=
ENST00000696032.1:c.3229T=	ENSP00000512341.1:p.Cys1077=
ENST00000696033.1:c.1160-36250T=	ENSP00000512342.1:n.1160-36250T=
ENST00000367429.9:c.3229T= MANE Select	ENSP00000356399.4:p.Cys1077=
ENST00000367429.8:c.3229T=	ENSP00000356399.4:p.Cys1077=
ENST00000466229.5:n.6327T=
NM_000186.3:c.3229T= , LRG_47t1:c.3229T=	NP_000177.2:p.Cys1077=
XR_001737134.2:n.3415T=
NM_000186.4:c.3229T= MANE Select	NP_000177.2:p.Cys1077=