Canonical Allele Identifier: CA343989112

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716401T>A (hg19) ; chr1:g.196747271T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747271T>A , CM000663.2:g.196747271T>A	GRCh38
NC_000001.10:g.196716401T>A , CM000663.1:g.196716401T>A	GRCh37
NC_000001.9:g.194983024T>A	NCBI36
NG_007259.1:g.100261T>A , LRG_47:g.100261T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4682T>A
ENST00000695970.1:c.3480T>A	ENSP00000512297.1:p.Cys1160Ter
ENST00000695971.1:c.3633T>A	ENSP00000512298.1:p.Cys1211Ter
ENST00000695972.1:c.*731T>A	ENSP00000512299.1:n.*731T>A
ENST00000695973.1:c.*2018T>A	ENSP00000512300.1:n.*2018T>A
ENST00000695974.1:c.3477T>A	ENSP00000512301.1:p.Cys1159Ter
ENST00000695975.1:c.*1781T>A	ENSP00000512302.1:n.*1781T>A
ENST00000695976.1:c.3465T>A	ENSP00000512303.1:p.Cys1155Ter
ENST00000695981.1:c.3580+74T>A	ENSP00000512306.1:n.3580+74T>A
ENST00000695984.1:c.1662T>A	ENSP00000512309.1:p.Cys554Ter
ENST00000695986.1:c.*3305T>A	ENSP00000512311.1:n.*3305T>A
ENST00000695990.1:n.688T>A
ENST00000696026.1:c.*1936T>A	ENSP00000512335.1:n.*1936T>A
ENST00000696027.1:c.3648T>A	ENSP00000512336.1:p.Cys1216Ter
ENST00000696028.1:c.3582T>A	ENSP00000512337.1:p.Cys1194Ter
ENST00000696029.1:c.3648T>A	ENSP00000512338.1:p.Cys1216Ter
ENST00000696031.1:c.*3172T>A	ENSP00000512340.1:n.*3172T>A
ENST00000696032.1:c.3580+74T>A	ENSP00000512341.1:n.3580+74T>A
ENST00000696033.1:c.1160-32526T>A	ENSP00000512342.1:n.1160-32526T>A
ENST00000367429.9:c.3654T>A MANE Select	ENSP00000356399.4:p.Cys1218Ter
ENST00000367429.8:c.3654T>A	ENSP00000356399.4:p.Cys1218Ter
ENST00000466229.5:n.6752T>A
NM_000186.3:c.3654T>A , LRG_47t1:c.3654T>A	NP_000177.2:p.Cys1218Ter
XR_001737134.2:n.3840T>A
NM_000186.4:c.3654T>A MANE Select	NP_000177.2:p.Cys1218Ter