Canonical Allele Identifier: CA343982985

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712606C>A (hg19) ; chr1:g.196743476C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743476C>A , CM000663.2:g.196743476C>A	GRCh38
NC_000001.10:g.196712606C>A , CM000663.1:g.196712606C>A	GRCh37
NC_000001.9:g.194979229C>A	NCBI36
NG_007259.1:g.96466C>A , LRG_47:g.96466C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4186C>A
ENST00000695970.1:c.2984C>A	ENSP00000512297.1:p.Thr995Lys
ENST00000695971.1:c.3137C>A	ENSP00000512298.1:p.Thr1046Lys
ENST00000695972.1:c.*235C>A	ENSP00000512299.1:n.*235C>A
ENST00000695973.1:c.*1522C>A	ENSP00000512300.1:n.*1522C>A
ENST00000695974.1:c.2981C>A	ENSP00000512301.1:p.Thr994Lys
ENST00000695975.1:c.*1285C>A	ENSP00000512302.1:n.*1285C>A
ENST00000695976.1:c.2969C>A	ENSP00000512303.1:p.Thr990Lys
ENST00000695981.1:c.3158C>A	ENSP00000512306.1:p.Thr1053Lys
ENST00000695984.1:c.1166C>A	ENSP00000512309.1:p.Thr389Lys
ENST00000695986.1:c.*2809C>A	ENSP00000512311.1:n.*2809C>A
ENST00000696026.1:c.*1440C>A	ENSP00000512335.1:n.*1440C>A
ENST00000696027.1:c.3152C>A	ENSP00000512336.1:p.Thr1051Lys
ENST00000696028.1:c.3086C>A	ENSP00000512337.1:p.Thr1029Lys
ENST00000696029.1:c.3152C>A	ENSP00000512338.1:p.Thr1051Lys
ENST00000696031.1:c.*2676C>A	ENSP00000512340.1:n.*2676C>A
ENST00000696032.1:c.3158C>A	ENSP00000512341.1:p.Thr1053Lys
ENST00000696033.1:c.1160-36321C>A	ENSP00000512342.1:n.1160-36321C>A
ENST00000367429.9:c.3158C>A MANE Select	ENSP00000356399.4:p.Thr1053Lys
ENST00000367429.8:c.3158C>A	ENSP00000356399.4:p.Thr1053Lys
ENST00000466229.5:n.6256C>A
NM_000186.3:c.3158C>A , LRG_47t1:c.3158C>A	NP_000177.2:p.Thr1053Lys
XR_001737134.2:n.3344C>A
NM_000186.4:c.3158C>A MANE Select	NP_000177.2:p.Thr1053Lys