Canonical Allele Identifier: CA1484711801
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109746309G= , CM000666.2:g.109746309G= GRCh38
NC_000004.11:g.110667465G= , CM000666.1:g.110667465G= GRCh37
NC_000004.10:g.110886914G= NCBI36
NG_007569.1:g.60677C= , LRG_48:g.60677C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1521C=
ENST00000695845.1:n.1520C=
ENST00000695846.1:n.1366C=
ENST00000394634.7:c.1342C= MANE Select ENSP00000378130.2:p.Arg448=
ENST00000394635.8:c.1366C= ENSP00000378131.3:p.Arg456=
ENST00000645635.1:c.1342C= ENSP00000493607.1:p.Arg448=
ENST00000394634.6:c.1342C= ENSP00000378130.2:p.Arg448=
ENST00000394635.7:c.1366C= ENSP00000378131.3:p.Arg456=
ENST00000504853.3:n.1759C=
ENST00000512148.5:c.1321C= ENSP00000427438.1:p.Arg441=
ENST00000618244.4:c.1044+3190C= ENSP00000483416.1:n.1044+3190C=
NM_000204.3:c.1342C= , LRG_48t1:c.1342C= NP_000195.2:p.Arg448=
XM_005262975.1:c.1366C= XP_005263032.1:p.Arg456=
XM_005262976.1:c.1321C= XP_005263033.1:p.Arg441=
XM_006714209.1:c.1363C= XP_006714272.1:p.Arg455=
XM_006714210.2:c.1366C= XP_006714273.1:p.Arg456=
XM_011531920.1:c.1366C= XP_011530222.1:p.Arg456=
NM_000204.4:c.1342C= NP_000195.2:p.Arg448=
NM_001318057.1:c.1366C= NP_001304986.1:p.Arg456=
NM_001331035.1:c.1321C= NP_001317964.1:p.Arg441=
XM_006714210.4:c.1366C= XP_006714273.1:p.Arg456=
XM_011531920.2:c.1366C= XP_011530222.1:p.Arg456=
XM_017008164.2:c.1342C= XP_016863653.1:p.Arg448=
XM_017008165.2:c.1321C= XP_016863654.1:p.Arg441=
XM_017008166.2:c.1342C= XP_016863655.1:p.Arg448=
NM_001318057.2:c.1366C= NP_001304986.2:p.Arg456=
NM_001331035.2:c.1321C= NP_001317964.1:p.Arg441=
NM_001375278.1:c.1366C= NP_001362207.1:p.Arg456=
NM_001375279.1:c.1342C= NP_001362208.1:p.Arg448=
NM_001375280.1:c.1321C= NP_001362209.1:p.Arg441=
NM_001375281.1:c.1342C= NP_001362210.1:p.Arg448=
NM_001375282.1:c.1321C= NP_001362211.1:p.Arg441=
NM_001375283.1:c.1285C= NP_001362212.1:p.Arg429=
NM_001375284.1:c.733C= NP_001362213.1:p.Arg245=
NR_164671.1:n.1176+2909C=
NR_164672.1:n.1392C=
NR_164673.1:n.1366C=
NM_000204.5:c.1342C= MANE Select NP_000195.3:p.Arg448=