Canonical Allele Identifier: CA343980186
Community Standard Title: NM_000186.4(CFH):c.1126C>T (p.Gln376Ter)
Gene: CFH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196689581C>T , CM000663.2:g.196689581C>T GRCh38
NC_000001.10:g.196658711C>T , CM000663.1:g.196658711C>T GRCh37
NC_000001.9:g.194925334C>T NCBI36
NG_007259.1:g.42571C>T , LRG_47:g.42571C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000186.4:c.1126C>T MANE Select NP_000177.2:p.Gln376Ter
ENST00000367429.9:c.1126C>T MANE Select ENSP00000356399.4:p.Gln376Ter
NM_000186.3:c.1126C>T , LRG_47t1:c.1126C>T NP_000177.2:p.Gln376Ter
NM_001014975.2:c.1126C>T NP_001014975.1:p.Gln376Ter
NM_001014975.3:c.1126C>T NP_001014975.1:p.Gln376Ter
ENST00000359637.2:c.934C>T ENSP00000352658.2:p.Gln312Ter
ENST00000359637.3:c.934C>T ENSP00000352658.2:p.Gln312Ter
ENST00000367429.8:c.1126C>T ENSP00000356399.4:p.Gln376Ter
ENST00000466229.5:n.3142C>T
ENST00000470918.2:n.1392C>T
ENST00000630130.2:c.1126C>T ENSP00000487250.1:p.Gln376Ter
ENST00000695968.1:c.943C>T ENSP00000512295.1:p.Gln315Ter
ENST00000695969.1:c.1126C>T ENSP00000512296.1:p.Gln376Ter
ENST00000695970.1:c.1126C>T ENSP00000512297.1:p.Gln376Ter
ENST00000695971.1:c.1105C>T ENSP00000512298.1:p.Gln369Ter
ENST00000695972.1:c.1126C>T ENSP00000512299.1:p.Gln376Ter
ENST00000695973.1:c.1126C>T ENSP00000512300.1:p.Gln376Ter
ENST00000695974.1:c.1126C>T ENSP00000512301.1:p.Gln376Ter
ENST00000695975.1:c.1126C>T ENSP00000512302.1:p.Gln376Ter
ENST00000695976.1:c.937C>T ENSP00000512303.1:p.Gln313Ter
ENST00000695978.1:c.1126C>T ENSP00000512304.1:p.Gln376Ter
ENST00000695979.1:c.1105C>T ENSP00000512305.1:p.Gln369Ter
ENST00000695980.1:n.1246C>T
ENST00000695981.1:c.1126C>T ENSP00000512306.1:p.Gln376Ter
ENST00000695983.1:c.1126C>T ENSP00000512308.1:p.Gln376Ter
ENST00000695984.1:c.244+16418C>T ENSP00000512309.1:n.244+16418C>T
ENST00000695986.1:c.*777C>T ENSP00000512311.1:n.*777C>T
ENST00000695987.1:c.937C>T ENSP00000512312.1:p.Gln313Ter
ENST00000696018.1:n.1210C>T
ENST00000696019.1:n.1210C>T
ENST00000696020.1:n.1210C>T
ENST00000696021.1:n.1189C>T
ENST00000696022.1:n.1210C>T
ENST00000696023.1:c.1126C>T ENSP00000512334.1:p.Gln376Ter
ENST00000696024.1:n.1210C>T
ENST00000696025.1:n.1210C>T
ENST00000696026.1:c.1126C>T ENSP00000512335.1:p.Gln376Ter
ENST00000696027.1:c.1126C>T ENSP00000512336.1:p.Gln376Ter
ENST00000696028.1:c.1126C>T ENSP00000512337.1:p.Gln376Ter
ENST00000696029.1:c.1126C>T ENSP00000512338.1:p.Gln376Ter
ENST00000696030.1:c.1051C>T ENSP00000512339.1:p.Gln351Ter
ENST00000696031.1:c.*644C>T ENSP00000512340.1:n.*644C>T
ENST00000696032.1:c.1126C>T ENSP00000512341.1:p.Gln376Ter
ENST00000696033.1:c.1126C>T ENSP00000512342.1:p.Gln376Ter
XM_017001108.2:c.1126C>T XP_016856597.1:p.Gln376Ter
XR_001737134.2:n.1211C>T