Canonical Allele Identifier: CA1484704989
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109740980G= , CM000666.2:g.109740980G= GRCh38
NC_000004.11:g.110662136G= , CM000666.1:g.110662136G= GRCh37
NC_000004.10:g.110881585G= NCBI36
NG_007569.1:g.66006C= , LRG_48:g.66006C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1713+1511C=
ENST00000695845.1:n.1712+1511C=
ENST00000695846.1:n.1689C=
ENST00000394634.7:c.1665C= MANE Select ENSP00000378130.2:p.Phe555=
ENST00000394635.8:c.1689C= ENSP00000378131.3:p.Phe563=
ENST00000645635.1:c.1534+1511C= ENSP00000493607.1:n.1534+1511C=
ENST00000394634.6:c.1665C= ENSP00000378130.2:p.Phe555=
ENST00000394635.7:c.1689C= ENSP00000378131.3:p.Phe563=
ENST00000504853.3:n.2082C=
ENST00000512148.5:c.1644C= ENSP00000427438.1:p.Phe548=
ENST00000618244.4:c.1045-175C= ENSP00000483416.1:n.1045-175C=
NM_000204.3:c.1665C= , LRG_48t1:c.1665C= NP_000195.2:p.Phe555=
XM_005262975.1:c.1689C= XP_005263032.1:p.Phe563=
XM_005262976.1:c.1644C= XP_005263033.1:p.Phe548=
XM_006714209.1:c.1686C= XP_006714272.1:p.Phe562=
XM_011531920.1:c.1558+1511C= XP_011530222.1:n.1558+1511C=
NM_000204.4:c.1665C= NP_000195.2:p.Phe555=
NM_001318057.1:c.1689C= NP_001304986.1:p.Phe563=
NM_001331035.1:c.1644C= NP_001317964.1:p.Phe548=
XM_011531920.2:c.1558+1511C= XP_011530222.1:n.1558+1511C=
XM_017008164.2:c.1534+1511C= XP_016863653.1:n.1534+1511C=
XM_017008165.2:c.1513+1511C= XP_016863654.1:n.1513+1511C=
XM_017008166.2:c.1534+1511C= XP_016863655.1:n.1534+1511C=
NM_001318057.2:c.1689C= NP_001304986.2:p.Phe563=
NM_001331035.2:c.1644C= NP_001317964.1:p.Phe548=
NM_001375278.1:c.1558+1511C= NP_001362207.1:n.1558+1511C=
NM_001375279.1:c.1534+1511C= NP_001362208.1:n.1534+1511C=
NM_001375280.1:c.1513+1511C= NP_001362209.1:n.1513+1511C=
NM_001375281.1:c.1534+1511C= NP_001362210.1:n.1534+1511C=
NM_001375282.1:c.1513+1511C= NP_001362211.1:n.1513+1511C=
NM_001375283.1:c.1608C= NP_001362212.1:p.Phe536=
NM_001375284.1:c.1056C= NP_001362213.1:p.Phe352=
NR_164671.1:n.1412C=
NR_164672.1:n.1715C=
NR_164673.1:n.1689C=
NM_000204.5:c.1665C= MANE Select NP_000195.3:p.Phe555=