Canonical Allele Identifier: CA1143770495

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196713816C= , CM000663.2:g.196713816C=	GRCh38
NC_000001.10:g.196682946C= , CM000663.1:g.196682946C=	GRCh37
NC_000001.9:g.194949569C=	NCBI36
NG_007259.1:g.66806C= , LRG_47:g.66806C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.1684C=
ENST00000695969.1:c.1418C=	ENSP00000512296.1:p.Ala473=
ENST00000695970.1:c.1418C=	ENSP00000512297.1:p.Ala473=
ENST00000695971.1:c.1397C=	ENSP00000512298.1:p.Ala466=
ENST00000695972.1:c.1418C=	ENSP00000512299.1:p.Ala473=
ENST00000695973.1:c.1418C=	ENSP00000512300.1:p.Ala473=
ENST00000695974.1:c.1418C=	ENSP00000512301.1:p.Ala473=
ENST00000695975.1:c.1418C=	ENSP00000512302.1:p.Ala473=
ENST00000695976.1:c.1229C=	ENSP00000512303.1:p.Ala410=
ENST00000695981.1:c.1418C=	ENSP00000512306.1:p.Ala473=
ENST00000695983.1:c.1418C=	ENSP00000512308.1:p.Ala473=
ENST00000695984.1:c.245-14530C=	ENSP00000512309.1:n.245-14530C=
ENST00000695986.1:c.*1069C=	ENSP00000512311.1:n.*1069C=
ENST00000696024.1:n.1502C=
ENST00000696025.1:n.1502C=
ENST00000696026.1:c.1418C=	ENSP00000512335.1:p.Ala473=
ENST00000696027.1:c.1418C=	ENSP00000512336.1:p.Ala473=
ENST00000696028.1:c.1418C=	ENSP00000512337.1:p.Ala473=
ENST00000696029.1:c.1418C=	ENSP00000512338.1:p.Ala473=
ENST00000696031.1:c.*936C=	ENSP00000512340.1:n.*936C=
ENST00000696032.1:c.1418C=	ENSP00000512341.1:p.Ala473=
ENST00000696033.1:c.1159+24202C=	ENSP00000512342.1:n.1159+24202C=
ENST00000367429.9:c.1418C= MANE Select	ENSP00000356399.4:p.Ala473=
ENST00000367429.8:c.1418C=	ENSP00000356399.4:p.Ala473=
ENST00000466229.5:n.3434C=
NM_000186.3:c.1418C= , LRG_47t1:c.1418C=	NP_000177.2:p.Ala473=
XR_001737134.2:n.1503C=
NM_000186.4:c.1418C= MANE Select	NP_000177.2:p.Ala473=