Canonical Allele Identifier: CA343984125

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712755A>T (hg19) ; chr1:g.196743625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743625A>T , CM000663.2:g.196743625A>T	GRCh38
NC_000001.10:g.196712755A>T , CM000663.1:g.196712755A>T	GRCh37
NC_000001.9:g.194979378A>T	NCBI36
NG_007259.1:g.96615A>T , LRG_47:g.96615A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4335A>T
ENST00000695970.1:c.3133A>T	ENSP00000512297.1:p.Lys1045Ter
ENST00000695971.1:c.3286A>T	ENSP00000512298.1:p.Lys1096Ter
ENST00000695972.1:c.*384A>T	ENSP00000512299.1:n.*384A>T
ENST00000695973.1:c.*1671A>T	ENSP00000512300.1:n.*1671A>T
ENST00000695974.1:c.3130A>T	ENSP00000512301.1:p.Lys1044Ter
ENST00000695975.1:c.*1434A>T	ENSP00000512302.1:n.*1434A>T
ENST00000695976.1:c.3118A>T	ENSP00000512303.1:p.Lys1040Ter
ENST00000695981.1:c.3307A>T	ENSP00000512306.1:p.Lys1103Ter
ENST00000695984.1:c.1315A>T	ENSP00000512309.1:p.Lys439Ter
ENST00000695986.1:c.*2958A>T	ENSP00000512311.1:n.*2958A>T
ENST00000696026.1:c.*1589A>T	ENSP00000512335.1:n.*1589A>T
ENST00000696027.1:c.3301A>T	ENSP00000512336.1:p.Lys1101Ter
ENST00000696028.1:c.3235A>T	ENSP00000512337.1:p.Lys1079Ter
ENST00000696029.1:c.3301A>T	ENSP00000512338.1:p.Lys1101Ter
ENST00000696031.1:c.*2825A>T	ENSP00000512340.1:n.*2825A>T
ENST00000696032.1:c.3307A>T	ENSP00000512341.1:p.Lys1103Ter
ENST00000696033.1:c.1160-36172A>T	ENSP00000512342.1:n.1160-36172A>T
ENST00000367429.9:c.3307A>T MANE Select	ENSP00000356399.4:p.Lys1103Ter
ENST00000367429.8:c.3307A>T	ENSP00000356399.4:p.Lys1103Ter
ENST00000466229.5:n.6405A>T
NM_000186.3:c.3307A>T , LRG_47t1:c.3307A>T	NP_000177.2:p.Lys1103Ter
XR_001737134.2:n.3493A>T
NM_000186.4:c.3307A>T MANE Select	NP_000177.2:p.Lys1103Ter