Canonical Allele Identifier: CA343986990

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716252A>T (hg19) ; chr1:g.196747122A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747122A>T , CM000663.2:g.196747122A>T	GRCh38
NC_000001.10:g.196716252A>T , CM000663.1:g.196716252A>T	GRCh37
NC_000001.9:g.194982875A>T	NCBI36
NG_007259.1:g.100112A>T , LRG_47:g.100112A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4533A>T
ENST00000695970.1:c.3331A>T	ENSP00000512297.1:p.Ile1111Leu
ENST00000695971.1:c.3484A>T	ENSP00000512298.1:p.Ile1162Leu
ENST00000695972.1:c.*582A>T	ENSP00000512299.1:n.*582A>T
ENST00000695973.1:c.*1869A>T	ENSP00000512300.1:n.*1869A>T
ENST00000695974.1:c.3328A>T	ENSP00000512301.1:p.Ile1110Leu
ENST00000695975.1:c.*1632A>T	ENSP00000512302.1:n.*1632A>T
ENST00000695976.1:c.3316A>T	ENSP00000512303.1:p.Ile1106Leu
ENST00000695981.1:c.3505A>T	ENSP00000512306.1:p.Ile1169Leu
ENST00000695984.1:c.1513A>T	ENSP00000512309.1:p.Ile505Leu
ENST00000695986.1:c.*3156A>T	ENSP00000512311.1:n.*3156A>T
ENST00000695990.1:n.539A>T
ENST00000696026.1:c.*1787A>T	ENSP00000512335.1:n.*1787A>T
ENST00000696027.1:c.3499A>T	ENSP00000512336.1:p.Ile1167Leu
ENST00000696028.1:c.3433A>T	ENSP00000512337.1:p.Ile1145Leu
ENST00000696029.1:c.3499A>T	ENSP00000512338.1:p.Ile1167Leu
ENST00000696031.1:c.*3023A>T	ENSP00000512340.1:n.*3023A>T
ENST00000696032.1:c.3505A>T	ENSP00000512341.1:p.Ile1169Leu
ENST00000696033.1:c.1160-32675A>T	ENSP00000512342.1:n.1160-32675A>T
ENST00000367429.9:c.3505A>T MANE Select	ENSP00000356399.4:p.Ile1169Leu
ENST00000367429.8:c.3505A>T	ENSP00000356399.4:p.Ile1169Leu
ENST00000466229.5:n.6603A>T
NM_000186.3:c.3505A>T , LRG_47t1:c.3505A>T	NP_000177.2:p.Ile1169Leu
XR_001737134.2:n.3691A>T
NM_000186.4:c.3505A>T MANE Select	NP_000177.2:p.Ile1169Leu