Canonical Allele Identifier: CA343983545

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712668C>A (hg19) ; chr1:g.196743538C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743538C>A , CM000663.2:g.196743538C>A	GRCh38
NC_000001.10:g.196712668C>A , CM000663.1:g.196712668C>A	GRCh37
NC_000001.9:g.194979291C>A	NCBI36
NG_007259.1:g.96528C>A , LRG_47:g.96528C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4248C>A
ENST00000695970.1:c.3046C>A	ENSP00000512297.1:p.Arg1016Ser
ENST00000695971.1:c.3199C>A	ENSP00000512298.1:p.Arg1067Ser
ENST00000695972.1:c.*297C>A	ENSP00000512299.1:n.*297C>A
ENST00000695973.1:c.*1584C>A	ENSP00000512300.1:n.*1584C>A
ENST00000695974.1:c.3043C>A	ENSP00000512301.1:p.Arg1015Ser
ENST00000695975.1:c.*1347C>A	ENSP00000512302.1:n.*1347C>A
ENST00000695976.1:c.3031C>A	ENSP00000512303.1:p.Arg1011Ser
ENST00000695981.1:c.3220C>A	ENSP00000512306.1:p.Arg1074Ser
ENST00000695984.1:c.1228C>A	ENSP00000512309.1:p.Arg410Ser
ENST00000695986.1:c.*2871C>A	ENSP00000512311.1:n.*2871C>A
ENST00000696026.1:c.*1502C>A	ENSP00000512335.1:n.*1502C>A
ENST00000696027.1:c.3214C>A	ENSP00000512336.1:p.Arg1072Ser
ENST00000696028.1:c.3148C>A	ENSP00000512337.1:p.Arg1050Ser
ENST00000696029.1:c.3214C>A	ENSP00000512338.1:p.Arg1072Ser
ENST00000696031.1:c.*2738C>A	ENSP00000512340.1:n.*2738C>A
ENST00000696032.1:c.3220C>A	ENSP00000512341.1:p.Arg1074Ser
ENST00000696033.1:c.1160-36259C>A	ENSP00000512342.1:n.1160-36259C>A
ENST00000367429.9:c.3220C>A MANE Select	ENSP00000356399.4:p.Arg1074Ser
ENST00000367429.8:c.3220C>A	ENSP00000356399.4:p.Arg1074Ser
ENST00000466229.5:n.6318C>A
NM_000186.3:c.3220C>A , LRG_47t1:c.3220C>A	NP_000177.2:p.Arg1074Ser
XR_001737134.2:n.3406C>A
NM_000186.4:c.3220C>A MANE Select	NP_000177.2:p.Arg1074Ser