Canonical Allele Identifier: CA343987938

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716343T>C (hg19) ; chr1:g.196747213T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747213T>C , CM000663.2:g.196747213T>C	GRCh38
NC_000001.10:g.196716343T>C , CM000663.1:g.196716343T>C	GRCh37
NC_000001.9:g.194982966T>C	NCBI36
NG_007259.1:g.100203T>C , LRG_47:g.100203T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4624T>C
ENST00000695970.1:c.3422T>C	ENSP00000512297.1:p.Phe1141Ser
ENST00000695971.1:c.3575T>C	ENSP00000512298.1:p.Phe1192Ser
ENST00000695972.1:c.*673T>C	ENSP00000512299.1:n.*673T>C
ENST00000695973.1:c.*1960T>C	ENSP00000512300.1:n.*1960T>C
ENST00000695974.1:c.3419T>C	ENSP00000512301.1:p.Phe1140Ser
ENST00000695975.1:c.*1723T>C	ENSP00000512302.1:n.*1723T>C
ENST00000695976.1:c.3407T>C	ENSP00000512303.1:p.Phe1136Ser
ENST00000695981.1:c.3580+16T>C	ENSP00000512306.1:n.3580+16T>C
ENST00000695984.1:c.1604T>C	ENSP00000512309.1:p.Phe535Ser
ENST00000695986.1:c.*3247T>C	ENSP00000512311.1:n.*3247T>C
ENST00000695990.1:n.630T>C
ENST00000696026.1:c.*1878T>C	ENSP00000512335.1:n.*1878T>C
ENST00000696027.1:c.3590T>C	ENSP00000512336.1:p.Phe1197Ser
ENST00000696028.1:c.3524T>C	ENSP00000512337.1:p.Phe1175Ser
ENST00000696029.1:c.3590T>C	ENSP00000512338.1:p.Phe1197Ser
ENST00000696031.1:c.*3114T>C	ENSP00000512340.1:n.*3114T>C
ENST00000696032.1:c.3580+16T>C	ENSP00000512341.1:n.3580+16T>C
ENST00000696033.1:c.1160-32584T>C	ENSP00000512342.1:n.1160-32584T>C
ENST00000367429.9:c.3596T>C MANE Select	ENSP00000356399.4:p.Phe1199Ser
ENST00000367429.8:c.3596T>C	ENSP00000356399.4:p.Phe1199Ser
ENST00000466229.5:n.6694T>C
NM_000186.3:c.3596T>C , LRG_47t1:c.3596T>C	NP_000177.2:p.Phe1199Ser
XR_001737134.2:n.3782T>C
NM_000186.4:c.3596T>C MANE Select	NP_000177.2:p.Phe1199Ser