Canonical Allele Identifier: CA1484705223
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109741107G= , CM000666.2:g.109741107G= GRCh38
NC_000004.11:g.110662263G= , CM000666.1:g.110662263G= GRCh37
NC_000004.10:g.110881712G= NCBI36
NG_007569.1:g.65879C= , LRG_48:g.65879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1713+1384C=
ENST00000695845.1:n.1712+1384C=
ENST00000695846.1:n.1562C=
ENST00000394634.7:c.1538C= MANE Select ENSP00000378130.2:p.Thr513=
ENST00000394635.8:c.1562C= ENSP00000378131.3:p.Thr521=
ENST00000645635.1:c.1534+1384C= ENSP00000493607.1:n.1534+1384C=
ENST00000394634.6:c.1538C= ENSP00000378130.2:p.Thr513=
ENST00000394635.7:c.1562C= ENSP00000378131.3:p.Thr521=
ENST00000504853.3:n.1955C=
ENST00000512148.5:c.1517C= ENSP00000427438.1:p.Thr506=
ENST00000618244.4:c.1045-302C= ENSP00000483416.1:n.1045-302C=
NM_000204.3:c.1538C= , LRG_48t1:c.1538C= NP_000195.2:p.Thr513=
XM_005262975.1:c.1562C= XP_005263032.1:p.Thr521=
XM_005262976.1:c.1517C= XP_005263033.1:p.Thr506=
XM_006714209.1:c.1559C= XP_006714272.1:p.Thr520=
XM_011531920.1:c.1558+1384C= XP_011530222.1:n.1558+1384C=
NM_000204.4:c.1538C= NP_000195.2:p.Thr513=
NM_001318057.1:c.1562C= NP_001304986.1:p.Thr521=
NM_001331035.1:c.1517C= NP_001317964.1:p.Thr506=
XM_011531920.2:c.1558+1384C= XP_011530222.1:n.1558+1384C=
XM_017008164.2:c.1534+1384C= XP_016863653.1:n.1534+1384C=
XM_017008165.2:c.1513+1384C= XP_016863654.1:n.1513+1384C=
XM_017008166.2:c.1534+1384C= XP_016863655.1:n.1534+1384C=
NM_001318057.2:c.1562C= NP_001304986.2:p.Thr521=
NM_001331035.2:c.1517C= NP_001317964.1:p.Thr506=
NM_001375278.1:c.1558+1384C= NP_001362207.1:n.1558+1384C=
NM_001375279.1:c.1534+1384C= NP_001362208.1:n.1534+1384C=
NM_001375280.1:c.1513+1384C= NP_001362209.1:n.1513+1384C=
NM_001375281.1:c.1534+1384C= NP_001362210.1:n.1534+1384C=
NM_001375282.1:c.1513+1384C= NP_001362211.1:n.1513+1384C=
NM_001375283.1:c.1481C= NP_001362212.1:p.Thr494=
NM_001375284.1:c.929C= NP_001362213.1:p.Thr310=
NR_164671.1:n.1285C=
NR_164672.1:n.1588C=
NR_164673.1:n.1562C=
NM_000204.5:c.1538C= MANE Select NP_000195.3:p.Thr513=