Canonical Allele Identifier: CA1484705014
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109740989T= , CM000666.2:g.109740989T= GRCh38
NC_000004.11:g.110662145T= , CM000666.1:g.110662145T= GRCh37
NC_000004.10:g.110881594T= NCBI36
NG_007569.1:g.65997A= , LRG_48:g.65997A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1713+1502A=
ENST00000695845.1:n.1712+1502A=
ENST00000695846.1:n.1680A=
ENST00000394634.7:c.1656A= MANE Select ENSP00000378130.2:p.Lys552=
ENST00000394635.8:c.1680A= ENSP00000378131.3:p.Lys560=
ENST00000645635.1:c.1534+1502A= ENSP00000493607.1:n.1534+1502A=
ENST00000394634.6:c.1656A= ENSP00000378130.2:p.Lys552=
ENST00000394635.7:c.1680A= ENSP00000378131.3:p.Lys560=
ENST00000504853.3:n.2073A=
ENST00000512148.5:c.1635A= ENSP00000427438.1:p.Lys545=
ENST00000618244.4:c.1045-184A= ENSP00000483416.1:n.1045-184A=
NM_000204.3:c.1656A= , LRG_48t1:c.1656A= NP_000195.2:p.Lys552=
XM_005262975.1:c.1680A= XP_005263032.1:p.Lys560=
XM_005262976.1:c.1635A= XP_005263033.1:p.Lys545=
XM_006714209.1:c.1677A= XP_006714272.1:p.Lys559=
XM_011531920.1:c.1558+1502A= XP_011530222.1:n.1558+1502A=
NM_000204.4:c.1656A= NP_000195.2:p.Lys552=
NM_001318057.1:c.1680A= NP_001304986.1:p.Lys560=
NM_001331035.1:c.1635A= NP_001317964.1:p.Lys545=
XM_011531920.2:c.1558+1502A= XP_011530222.1:n.1558+1502A=
XM_017008164.2:c.1534+1502A= XP_016863653.1:n.1534+1502A=
XM_017008165.2:c.1513+1502A= XP_016863654.1:n.1513+1502A=
XM_017008166.2:c.1534+1502A= XP_016863655.1:n.1534+1502A=
NM_001318057.2:c.1680A= NP_001304986.2:p.Lys560=
NM_001331035.2:c.1635A= NP_001317964.1:p.Lys545=
NM_001375278.1:c.1558+1502A= NP_001362207.1:n.1558+1502A=
NM_001375279.1:c.1534+1502A= NP_001362208.1:n.1534+1502A=
NM_001375280.1:c.1513+1502A= NP_001362209.1:n.1513+1502A=
NM_001375281.1:c.1534+1502A= NP_001362210.1:n.1534+1502A=
NM_001375282.1:c.1513+1502A= NP_001362211.1:n.1513+1502A=
NM_001375283.1:c.1599A= NP_001362212.1:p.Lys533=
NM_001375284.1:c.1047A= NP_001362213.1:p.Lys349=
NR_164671.1:n.1403A=
NR_164672.1:n.1706A=
NR_164673.1:n.1680A=
NM_000204.5:c.1656A= MANE Select NP_000195.3:p.Lys552=