Canonical Allele Identifier: CA1217768965

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743457T= , CM000663.2:g.196743457T=	GRCh38
NC_000001.10:g.196712587T= , CM000663.1:g.196712587T=	GRCh37
NC_000001.9:g.194979210T=	NCBI36
NG_007259.1:g.96447T= , LRG_47:g.96447T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4167T=
ENST00000695970.1:c.2965T=	ENSP00000512297.1:p.Ser989=
ENST00000695971.1:c.3118T=	ENSP00000512298.1:p.Ser1040=
ENST00000695972.1:c.*216T=	ENSP00000512299.1:n.*216T=
ENST00000695973.1:c.*1503T=	ENSP00000512300.1:n.*1503T=
ENST00000695974.1:c.2962T=	ENSP00000512301.1:p.Ser988=
ENST00000695975.1:c.*1266T=	ENSP00000512302.1:n.*1266T=
ENST00000695976.1:c.2950T=	ENSP00000512303.1:p.Ser984=
ENST00000695981.1:c.3139T=	ENSP00000512306.1:p.Ser1047=
ENST00000695984.1:c.1147T=	ENSP00000512309.1:p.Ser383=
ENST00000695986.1:c.*2790T=	ENSP00000512311.1:n.*2790T=
ENST00000696026.1:c.*1421T=	ENSP00000512335.1:n.*1421T=
ENST00000696027.1:c.3133T=	ENSP00000512336.1:p.Ser1045=
ENST00000696028.1:c.3067T=	ENSP00000512337.1:p.Ser1023=
ENST00000696029.1:c.3133T=	ENSP00000512338.1:p.Ser1045=
ENST00000696031.1:c.*2657T=	ENSP00000512340.1:n.*2657T=
ENST00000696032.1:c.3139T=	ENSP00000512341.1:p.Ser1047=
ENST00000696033.1:c.1160-36340T=	ENSP00000512342.1:n.1160-36340T=
ENST00000367429.9:c.3139T= MANE Select	ENSP00000356399.4:p.Ser1047=
ENST00000367429.8:c.3139T=	ENSP00000356399.4:p.Ser1047=
ENST00000466229.5:n.6237T=
NM_000186.3:c.3139T= , LRG_47t1:c.3139T=	NP_000177.2:p.Ser1047=
XR_001737134.2:n.3325T=
NM_000186.4:c.3139T= MANE Select	NP_000177.2:p.Ser1047=