Canonical Allele Identifier: CA1484705130
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109741062G= , CM000666.2:g.109741062G= GRCh38
NC_000004.11:g.110662218G= , CM000666.1:g.110662218G= GRCh37
NC_000004.10:g.110881667G= NCBI36
NG_007569.1:g.65924C= , LRG_48:g.65924C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1713+1429C=
ENST00000695845.1:n.1712+1429C=
ENST00000695846.1:n.1607C=
ENST00000394634.7:c.1583C= MANE Select ENSP00000378130.2:p.Pro528=
ENST00000394635.8:c.1607C= ENSP00000378131.3:p.Pro536=
ENST00000645635.1:c.1534+1429C= ENSP00000493607.1:n.1534+1429C=
ENST00000394634.6:c.1583C= ENSP00000378130.2:p.Pro528=
ENST00000394635.7:c.1607C= ENSP00000378131.3:p.Pro536=
ENST00000504853.3:n.2000C=
ENST00000512148.5:c.1562C= ENSP00000427438.1:p.Pro521=
ENST00000618244.4:c.1045-257C= ENSP00000483416.1:n.1045-257C=
NM_000204.3:c.1583C= , LRG_48t1:c.1583C= NP_000195.2:p.Pro528=
XM_005262975.1:c.1607C= XP_005263032.1:p.Pro536=
XM_005262976.1:c.1562C= XP_005263033.1:p.Pro521=
XM_006714209.1:c.1604C= XP_006714272.1:p.Pro535=
XM_011531920.1:c.1558+1429C= XP_011530222.1:n.1558+1429C=
NM_000204.4:c.1583C= NP_000195.2:p.Pro528=
NM_001318057.1:c.1607C= NP_001304986.1:p.Pro536=
NM_001331035.1:c.1562C= NP_001317964.1:p.Pro521=
XM_011531920.2:c.1558+1429C= XP_011530222.1:n.1558+1429C=
XM_017008164.2:c.1534+1429C= XP_016863653.1:n.1534+1429C=
XM_017008165.2:c.1513+1429C= XP_016863654.1:n.1513+1429C=
XM_017008166.2:c.1534+1429C= XP_016863655.1:n.1534+1429C=
NM_001318057.2:c.1607C= NP_001304986.2:p.Pro536=
NM_001331035.2:c.1562C= NP_001317964.1:p.Pro521=
NM_001375278.1:c.1558+1429C= NP_001362207.1:n.1558+1429C=
NM_001375279.1:c.1534+1429C= NP_001362208.1:n.1534+1429C=
NM_001375280.1:c.1513+1429C= NP_001362209.1:n.1513+1429C=
NM_001375281.1:c.1534+1429C= NP_001362210.1:n.1534+1429C=
NM_001375282.1:c.1513+1429C= NP_001362211.1:n.1513+1429C=
NM_001375283.1:c.1526C= NP_001362212.1:p.Pro509=
NM_001375284.1:c.974C= NP_001362213.1:p.Pro325=
NR_164671.1:n.1330C=
NR_164672.1:n.1633C=
NR_164673.1:n.1607C=
NM_000204.5:c.1583C= MANE Select NP_000195.3:p.Pro528=