Canonical Allele Identifier: CA1217770814

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747352G= , CM000663.2:g.196747352G=	GRCh38
NC_000001.10:g.196716482G= , CM000663.1:g.196716482G=	GRCh37
NC_000001.9:g.194983105G=	NCBI36
NG_007259.1:g.100342G= , LRG_47:g.100342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4763G=
ENST00000695970.1:c.*39G=	ENSP00000512297.1:n.*39G=
ENST00000695971.1:c.*39G=	ENSP00000512298.1:n.*39G=
ENST00000695972.1:c.*812G=	ENSP00000512299.1:n.*812G=
ENST00000695973.1:c.*2099G=	ENSP00000512300.1:n.*2099G=
ENST00000695974.1:c.*39G=	ENSP00000512301.1:n.*39G=
ENST00000695975.1:c.*1862G=	ENSP00000512302.1:n.*1862G=
ENST00000695976.1:c.*39G=	ENSP00000512303.1:n.*39G=
ENST00000695981.1:c.3580+155G=	ENSP00000512306.1:n.3580+155G=
ENST00000695984.1:c.*39G=	ENSP00000512309.1:n.*39G=
ENST00000695986.1:c.*3386G=	ENSP00000512311.1:n.*3386G=
ENST00000695990.1:n.769G=
ENST00000696026.1:c.*2017G=	ENSP00000512335.1:n.*2017G=
ENST00000696027.1:c.*39G=	ENSP00000512336.1:n.*39G=
ENST00000696028.1:c.*39G=	ENSP00000512337.1:n.*39G=
ENST00000696029.1:c.*39G=	ENSP00000512338.1:n.*39G=
ENST00000696031.1:c.*3253G=	ENSP00000512340.1:n.*3253G=
ENST00000696032.1:c.3580+155G=	ENSP00000512341.1:n.3580+155G=
ENST00000696033.1:c.1160-32445G=	ENSP00000512342.1:n.1160-32445G=
ENST00000367429.9:c.*39G= MANE Select	ENSP00000356399.4:n.*39G=
ENST00000367429.8:c.*39G=	ENSP00000356399.4:n.*39G=
ENST00000466229.5:n.6833G=
NM_000186.3:c.*39G= , LRG_47t1:c.*39G=	NP_000177.2:n.*39G=
XR_001737134.2:n.3921G=
NM_000186.4:c.*39G= MANE Select	NP_000177.2:n.*39G=