Canonical Allele Identifier: CA1010872537
Gene: CFH HGNC NCBI

Linked Data

dbSNP Id: rs1653039850

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196747126_196747138del , CM000663.2:g.196747126_196747138del GRCh38
NC_000001.10:g.196716256_196716268del , CM000663.1:g.196716256_196716268del GRCh37
NC_000001.9:g.194982879_194982891del NCBI36
NG_007259.1:g.100116_100128del , LRG_47:g.100116_100128del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470918.2:n.4537_4549del
ENST00000695970.1:c.3335_3347del ENSP00000512297.1:p.Ser1112TrpfsTer6
ENST00000695971.1:c.3488_3500del ENSP00000512298.1:p.Ser1163TrpfsTer6
ENST00000695972.1:c.*586_*598del ENSP00000512299.1:n.*586_*598del
ENST00000695973.1:c.*1873_*1885del ENSP00000512300.1:n.*1873_*1885del
ENST00000695974.1:c.3332_3344del ENSP00000512301.1:p.Ser1111TrpfsTer6
ENST00000695975.1:c.*1636_*1648del ENSP00000512302.1:n.*1636_*1648del
ENST00000695976.1:c.3320_3332del ENSP00000512303.1:p.Ser1107TrpfsTer6
ENST00000695981.1:c.3509_3521del ENSP00000512306.1:p.Ser1170TrpfsTer6
ENST00000695984.1:c.1517_1529del ENSP00000512309.1:p.Ser506TrpfsTer6
ENST00000695986.1:c.*3160_*3172del ENSP00000512311.1:n.*3160_*3172del
ENST00000695990.1:n.543_555del
ENST00000696026.1:c.*1791_*1803del ENSP00000512335.1:n.*1791_*1803del
ENST00000696027.1:c.3503_3515del ENSP00000512336.1:p.Ser1168TrpfsTer6
ENST00000696028.1:c.3437_3449del ENSP00000512337.1:p.Ser1146TrpfsTer6
ENST00000696029.1:c.3503_3515del ENSP00000512338.1:p.Ser1168TrpfsTer6
ENST00000696031.1:c.*3027_*3039del ENSP00000512340.1:n.*3027_*3039del
ENST00000696032.1:c.3509_3521del ENSP00000512341.1:p.Ser1170TrpfsTer6
ENST00000696033.1:c.1160-32671_1160-32659del ENSP00000512342.1:n.1160-32671_1160-32659del
ENST00000367429.9:c.3509_3521del MANE Select ENSP00000356399.4:p.Ser1170TrpfsTer6
ENST00000367429.8:c.3509_3521del ENSP00000356399.4:p.Ser1170TrpfsTer6
ENST00000466229.5:n.6607_6619del
NM_000186.3:c.3509_3521del , LRG_47t1:c.3509_3521del NP_000177.2:p.Ser1170TrpfsTer6
XR_001737134.2:n.3695_3707del
NM_000186.4:c.3509_3521del MANE Select NP_000177.2:p.Ser1170TrpfsTer6