Canonical Allele Identifier: CA1217770815

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747356T= , CM000663.2:g.196747356T=	GRCh38
NC_000001.10:g.196716486T= , CM000663.1:g.196716486T=	GRCh37
NC_000001.9:g.194983109T=	NCBI36
NG_007259.1:g.100346T= , LRG_47:g.100346T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4767T=
ENST00000695970.1:c.*43T=	ENSP00000512297.1:n.*43T=
ENST00000695971.1:c.*43T=	ENSP00000512298.1:n.*43T=
ENST00000695972.1:c.*816T=	ENSP00000512299.1:n.*816T=
ENST00000695973.1:c.*2103T=	ENSP00000512300.1:n.*2103T=
ENST00000695974.1:c.*43T=	ENSP00000512301.1:n.*43T=
ENST00000695975.1:c.*1866T=	ENSP00000512302.1:n.*1866T=
ENST00000695976.1:c.*43T=	ENSP00000512303.1:n.*43T=
ENST00000695981.1:c.3580+159T=	ENSP00000512306.1:n.3580+159T=
ENST00000695984.1:c.*43T=	ENSP00000512309.1:n.*43T=
ENST00000695986.1:c.*3390T=	ENSP00000512311.1:n.*3390T=
ENST00000695990.1:n.773T=
ENST00000696026.1:c.*2021T=	ENSP00000512335.1:n.*2021T=
ENST00000696027.1:c.*43T=	ENSP00000512336.1:n.*43T=
ENST00000696028.1:c.*43T=	ENSP00000512337.1:n.*43T=
ENST00000696029.1:c.*43T=	ENSP00000512338.1:n.*43T=
ENST00000696031.1:c.*3257T=	ENSP00000512340.1:n.*3257T=
ENST00000696032.1:c.3580+159T=	ENSP00000512341.1:n.3580+159T=
ENST00000696033.1:c.1160-32441T=	ENSP00000512342.1:n.1160-32441T=
ENST00000367429.9:c.*43T= MANE Select	ENSP00000356399.4:n.*43T=
ENST00000367429.8:c.*43T=	ENSP00000356399.4:n.*43T=
ENST00000466229.5:n.6837T=
NM_000186.3:c.*43T= , LRG_47t1:c.*43T=	NP_000177.2:n.*43T=
XR_001737134.2:n.3925T=
NM_000186.4:c.*43T= MANE Select	NP_000177.2:n.*43T=