Canonical Allele Identifier: CA343986971

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716248T>G (hg19) ; chr1:g.196747118T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747118T>G , CM000663.2:g.196747118T>G	GRCh38
NC_000001.10:g.196716248T>G , CM000663.1:g.196716248T>G	GRCh37
NC_000001.9:g.194982871T>G	NCBI36
NG_007259.1:g.100108T>G , LRG_47:g.100108T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4529T>G
ENST00000695970.1:c.3327T>G	ENSP00000512297.1:p.Cys1109Trp
ENST00000695971.1:c.3480T>G	ENSP00000512298.1:p.Cys1160Trp
ENST00000695972.1:c.*578T>G	ENSP00000512299.1:n.*578T>G
ENST00000695973.1:c.*1865T>G	ENSP00000512300.1:n.*1865T>G
ENST00000695974.1:c.3324T>G	ENSP00000512301.1:p.Cys1108Trp
ENST00000695975.1:c.*1628T>G	ENSP00000512302.1:n.*1628T>G
ENST00000695976.1:c.3312T>G	ENSP00000512303.1:p.Cys1104Trp
ENST00000695981.1:c.3501T>G	ENSP00000512306.1:p.Cys1167Trp
ENST00000695984.1:c.1509T>G	ENSP00000512309.1:p.Cys503Trp
ENST00000695986.1:c.*3152T>G	ENSP00000512311.1:n.*3152T>G
ENST00000695990.1:n.535T>G
ENST00000696026.1:c.*1783T>G	ENSP00000512335.1:n.*1783T>G
ENST00000696027.1:c.3495T>G	ENSP00000512336.1:p.Cys1165Trp
ENST00000696028.1:c.3429T>G	ENSP00000512337.1:p.Cys1143Trp
ENST00000696029.1:c.3495T>G	ENSP00000512338.1:p.Cys1165Trp
ENST00000696031.1:c.*3019T>G	ENSP00000512340.1:n.*3019T>G
ENST00000696032.1:c.3501T>G	ENSP00000512341.1:p.Cys1167Trp
ENST00000696033.1:c.1160-32679T>G	ENSP00000512342.1:n.1160-32679T>G
ENST00000367429.9:c.3501T>G MANE Select	ENSP00000356399.4:p.Cys1167Trp
ENST00000367429.8:c.3501T>G	ENSP00000356399.4:p.Cys1167Trp
ENST00000466229.5:n.6599T>G
NM_000186.3:c.3501T>G , LRG_47t1:c.3501T>G	NP_000177.2:p.Cys1167Trp
XR_001737134.2:n.3687T>G
NM_000186.4:c.3501T>G MANE Select	NP_000177.2:p.Cys1167Trp