Canonical Allele Identifier: CA1484704915
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109740930T= , CM000666.2:g.109740930T= GRCh38
NC_000004.11:g.110662086T= , CM000666.1:g.110662086T= GRCh37
NC_000004.10:g.110881535T= NCBI36
NG_007569.1:g.66056A= , LRG_48:g.66056A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1713+1561A=
ENST00000695845.1:n.1712+1561A=
ENST00000695846.1:n.1739A=
ENST00000394634.7:c.1715A= MANE Select ENSP00000378130.2:p.His572=
ENST00000394635.8:c.1739A= ENSP00000378131.3:p.His580=
ENST00000645635.1:c.1534+1561A= ENSP00000493607.1:n.1534+1561A=
ENST00000394634.6:c.1715A= ENSP00000378130.2:p.His572=
ENST00000394635.7:c.1739A= ENSP00000378131.3:p.His580=
ENST00000504853.3:n.2132A=
ENST00000512148.5:c.1694A= ENSP00000427438.1:p.His565=
ENST00000618244.4:c.1045-125A= ENSP00000483416.1:n.1045-125A=
NM_000204.3:c.1715A= , LRG_48t1:c.1715A= NP_000195.2:p.His572=
XM_005262975.1:c.1739A= XP_005263032.1:p.His580=
XM_005262976.1:c.1694A= XP_005263033.1:p.His565=
XM_006714209.1:c.1736A= XP_006714272.1:p.His579=
XM_011531920.1:c.1558+1561A= XP_011530222.1:n.1558+1561A=
NM_000204.4:c.1715A= NP_000195.2:p.His572=
NM_001318057.1:c.1739A= NP_001304986.1:p.His580=
NM_001331035.1:c.1694A= NP_001317964.1:p.His565=
XM_011531920.2:c.1558+1561A= XP_011530222.1:n.1558+1561A=
XM_017008164.2:c.1534+1561A= XP_016863653.1:n.1534+1561A=
XM_017008165.2:c.1513+1561A= XP_016863654.1:n.1513+1561A=
XM_017008166.2:c.1534+1561A= XP_016863655.1:n.1534+1561A=
NM_001318057.2:c.1739A= NP_001304986.2:p.His580=
NM_001331035.2:c.1694A= NP_001317964.1:p.His565=
NM_001375278.1:c.1558+1561A= NP_001362207.1:n.1558+1561A=
NM_001375279.1:c.1534+1561A= NP_001362208.1:n.1534+1561A=
NM_001375280.1:c.1513+1561A= NP_001362209.1:n.1513+1561A=
NM_001375281.1:c.1534+1561A= NP_001362210.1:n.1534+1561A=
NM_001375282.1:c.1513+1561A= NP_001362211.1:n.1513+1561A=
NM_001375283.1:c.1658A= NP_001362212.1:p.His553=
NM_001375284.1:c.1106A= NP_001362213.1:p.His369=
NR_164671.1:n.1462A=
NR_164672.1:n.1765A=
NR_164673.1:n.1739A=
NM_000204.5:c.1715A= MANE Select NP_000195.3:p.His572=