Canonical Allele Identifier: CA1484705150
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109741076C= , CM000666.2:g.109741076C= GRCh38
NC_000004.11:g.110662232C= , CM000666.1:g.110662232C= GRCh37
NC_000004.10:g.110881681C= NCBI36
NG_007569.1:g.65910G= , LRG_48:g.65910G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1713+1415G=
ENST00000695845.1:n.1712+1415G=
ENST00000695846.1:n.1593G=
ENST00000394634.7:c.1569G= MANE Select ENSP00000378130.2:p.Gly523=
ENST00000394635.8:c.1593G= ENSP00000378131.3:p.Gly531=
ENST00000645635.1:c.1534+1415G= ENSP00000493607.1:n.1534+1415G=
ENST00000394634.6:c.1569G= ENSP00000378130.2:p.Gly523=
ENST00000394635.7:c.1593G= ENSP00000378131.3:p.Gly531=
ENST00000504853.3:n.1986G=
ENST00000512148.5:c.1548G= ENSP00000427438.1:p.Gly516=
ENST00000618244.4:c.1045-271G= ENSP00000483416.1:n.1045-271G=
NM_000204.3:c.1569G= , LRG_48t1:c.1569G= NP_000195.2:p.Gly523=
XM_005262975.1:c.1593G= XP_005263032.1:p.Gly531=
XM_005262976.1:c.1548G= XP_005263033.1:p.Gly516=
XM_006714209.1:c.1590G= XP_006714272.1:p.Gly530=
XM_011531920.1:c.1558+1415G= XP_011530222.1:n.1558+1415G=
NM_000204.4:c.1569G= NP_000195.2:p.Gly523=
NM_001318057.1:c.1593G= NP_001304986.1:p.Gly531=
NM_001331035.1:c.1548G= NP_001317964.1:p.Gly516=
XM_011531920.2:c.1558+1415G= XP_011530222.1:n.1558+1415G=
XM_017008164.2:c.1534+1415G= XP_016863653.1:n.1534+1415G=
XM_017008165.2:c.1513+1415G= XP_016863654.1:n.1513+1415G=
XM_017008166.2:c.1534+1415G= XP_016863655.1:n.1534+1415G=
NM_001318057.2:c.1593G= NP_001304986.2:p.Gly531=
NM_001331035.2:c.1548G= NP_001317964.1:p.Gly516=
NM_001375278.1:c.1558+1415G= NP_001362207.1:n.1558+1415G=
NM_001375279.1:c.1534+1415G= NP_001362208.1:n.1534+1415G=
NM_001375280.1:c.1513+1415G= NP_001362209.1:n.1513+1415G=
NM_001375281.1:c.1534+1415G= NP_001362210.1:n.1534+1415G=
NM_001375282.1:c.1513+1415G= NP_001362211.1:n.1513+1415G=
NM_001375283.1:c.1512G= NP_001362212.1:p.Gly504=
NM_001375284.1:c.960G= NP_001362213.1:p.Gly320=
NR_164671.1:n.1316G=
NR_164672.1:n.1619G=
NR_164673.1:n.1593G=
NM_000204.5:c.1569G= MANE Select NP_000195.3:p.Gly523=