Canonical Allele Identifier: CA343987545

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716306C>A (hg19) ; chr1:g.196747176C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747176C>A , CM000663.2:g.196747176C>A	GRCh38
NC_000001.10:g.196716306C>A , CM000663.1:g.196716306C>A	GRCh37
NC_000001.9:g.194982929C>A	NCBI36
NG_007259.1:g.100166C>A , LRG_47:g.100166C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4587C>A
ENST00000695970.1:c.3385C>A	ENSP00000512297.1:p.Gln1129Lys
ENST00000695971.1:c.3538C>A	ENSP00000512298.1:p.Gln1180Lys
ENST00000695972.1:c.*636C>A	ENSP00000512299.1:n.*636C>A
ENST00000695973.1:c.*1923C>A	ENSP00000512300.1:n.*1923C>A
ENST00000695974.1:c.3382C>A	ENSP00000512301.1:p.Gln1128Lys
ENST00000695975.1:c.*1686C>A	ENSP00000512302.1:n.*1686C>A
ENST00000695976.1:c.3370C>A	ENSP00000512303.1:p.Gln1124Lys
ENST00000695981.1:c.3559C>A	ENSP00000512306.1:p.Gln1187Lys
ENST00000695984.1:c.1567C>A	ENSP00000512309.1:p.Gln523Lys
ENST00000695986.1:c.*3210C>A	ENSP00000512311.1:n.*3210C>A
ENST00000695990.1:n.593C>A
ENST00000696026.1:c.*1841C>A	ENSP00000512335.1:n.*1841C>A
ENST00000696027.1:c.3553C>A	ENSP00000512336.1:p.Gln1185Lys
ENST00000696028.1:c.3487C>A	ENSP00000512337.1:p.Gln1163Lys
ENST00000696029.1:c.3553C>A	ENSP00000512338.1:p.Gln1185Lys
ENST00000696031.1:c.*3077C>A	ENSP00000512340.1:n.*3077C>A
ENST00000696032.1:c.3559C>A	ENSP00000512341.1:p.Gln1187Lys
ENST00000696033.1:c.1160-32621C>A	ENSP00000512342.1:n.1160-32621C>A
ENST00000367429.9:c.3559C>A MANE Select	ENSP00000356399.4:p.Gln1187Lys
ENST00000367429.8:c.3559C>A	ENSP00000356399.4:p.Gln1187Lys
ENST00000466229.5:n.6657C>A
NM_000186.3:c.3559C>A , LRG_47t1:c.3559C>A	NP_000177.2:p.Gln1187Lys
XR_001737134.2:n.3745C>A
NM_000186.4:c.3559C>A MANE Select	NP_000177.2:p.Gln1187Lys