Canonical Allele Identifier: CA343983412

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712648A>T (hg19) ; chr1:g.196743518A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743518A>T , CM000663.2:g.196743518A>T	GRCh38
NC_000001.10:g.196712648A>T , CM000663.1:g.196712648A>T	GRCh37
NC_000001.9:g.194979271A>T	NCBI36
NG_007259.1:g.96508A>T , LRG_47:g.96508A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4228A>T
ENST00000695970.1:c.3026A>T	ENSP00000512297.1:p.Tyr1009Phe
ENST00000695971.1:c.3179A>T	ENSP00000512298.1:p.Tyr1060Phe
ENST00000695972.1:c.*277A>T	ENSP00000512299.1:n.*277A>T
ENST00000695973.1:c.*1564A>T	ENSP00000512300.1:n.*1564A>T
ENST00000695974.1:c.3023A>T	ENSP00000512301.1:p.Tyr1008Phe
ENST00000695975.1:c.*1327A>T	ENSP00000512302.1:n.*1327A>T
ENST00000695976.1:c.3011A>T	ENSP00000512303.1:p.Tyr1004Phe
ENST00000695981.1:c.3200A>T	ENSP00000512306.1:p.Tyr1067Phe
ENST00000695984.1:c.1208A>T	ENSP00000512309.1:p.Tyr403Phe
ENST00000695986.1:c.*2851A>T	ENSP00000512311.1:n.*2851A>T
ENST00000696026.1:c.*1482A>T	ENSP00000512335.1:n.*1482A>T
ENST00000696027.1:c.3194A>T	ENSP00000512336.1:p.Tyr1065Phe
ENST00000696028.1:c.3128A>T	ENSP00000512337.1:p.Tyr1043Phe
ENST00000696029.1:c.3194A>T	ENSP00000512338.1:p.Tyr1065Phe
ENST00000696031.1:c.*2718A>T	ENSP00000512340.1:n.*2718A>T
ENST00000696032.1:c.3200A>T	ENSP00000512341.1:p.Tyr1067Phe
ENST00000696033.1:c.1160-36279A>T	ENSP00000512342.1:n.1160-36279A>T
ENST00000367429.9:c.3200A>T MANE Select	ENSP00000356399.4:p.Tyr1067Phe
ENST00000367429.8:c.3200A>T	ENSP00000356399.4:p.Tyr1067Phe
ENST00000466229.5:n.6298A>T
NM_000186.3:c.3200A>T , LRG_47t1:c.3200A>T	NP_000177.2:p.Tyr1067Phe
XR_001737134.2:n.3386A>T
NM_000186.4:c.3200A>T MANE Select	NP_000177.2:p.Tyr1067Phe