Canonical Allele Identifier: CA1484711788
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109746305G= , CM000666.2:g.109746305G= GRCh38
NC_000004.11:g.110667461G= , CM000666.1:g.110667461G= GRCh37
NC_000004.10:g.110886910G= NCBI36
NG_007569.1:g.60681C= , LRG_48:g.60681C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1525C=
ENST00000695845.1:n.1524C=
ENST00000695846.1:n.1370C=
ENST00000394634.7:c.1346C= MANE Select ENSP00000378130.2:p.Ser449=
ENST00000394635.8:c.1370C= ENSP00000378131.3:p.Ser457=
ENST00000645635.1:c.1346C= ENSP00000493607.1:p.Ser449=
ENST00000394634.6:c.1346C= ENSP00000378130.2:p.Ser449=
ENST00000394635.7:c.1370C= ENSP00000378131.3:p.Ser457=
ENST00000504853.3:n.1763C=
ENST00000512148.5:c.1325C= ENSP00000427438.1:p.Ser442=
ENST00000618244.4:c.1044+3194C= ENSP00000483416.1:n.1044+3194C=
NM_000204.3:c.1346C= , LRG_48t1:c.1346C= NP_000195.2:p.Ser449=
XM_005262975.1:c.1370C= XP_005263032.1:p.Ser457=
XM_005262976.1:c.1325C= XP_005263033.1:p.Ser442=
XM_006714209.1:c.1367C= XP_006714272.1:p.Ser456=
XM_006714210.2:c.1370C= XP_006714273.1:p.Ser457=
XM_011531920.1:c.1370C= XP_011530222.1:p.Ser457=
NM_000204.4:c.1346C= NP_000195.2:p.Ser449=
NM_001318057.1:c.1370C= NP_001304986.1:p.Ser457=
NM_001331035.1:c.1325C= NP_001317964.1:p.Ser442=
XM_006714210.4:c.1370C= XP_006714273.1:p.Ser457=
XM_011531920.2:c.1370C= XP_011530222.1:p.Ser457=
XM_017008164.2:c.1346C= XP_016863653.1:p.Ser449=
XM_017008165.2:c.1325C= XP_016863654.1:p.Ser442=
XM_017008166.2:c.1346C= XP_016863655.1:p.Ser449=
NM_001318057.2:c.1370C= NP_001304986.2:p.Ser457=
NM_001331035.2:c.1325C= NP_001317964.1:p.Ser442=
NM_001375278.1:c.1370C= NP_001362207.1:p.Ser457=
NM_001375279.1:c.1346C= NP_001362208.1:p.Ser449=
NM_001375280.1:c.1325C= NP_001362209.1:p.Ser442=
NM_001375281.1:c.1346C= NP_001362210.1:p.Ser449=
NM_001375282.1:c.1325C= NP_001362211.1:p.Ser442=
NM_001375283.1:c.1289C= NP_001362212.1:p.Ser430=
NM_001375284.1:c.737C= NP_001362213.1:p.Ser246=
NR_164671.1:n.1176+2913C=
NR_164672.1:n.1396C=
NR_164673.1:n.1370C=
NM_000204.5:c.1346C= MANE Select NP_000195.3:p.Ser449=