Canonical Allele Identifier: CA1484716238
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109749608A= , CM000666.2:g.109749608A= GRCh38
NC_000004.11:g.110670764A= , CM000666.1:g.110670764A= GRCh37
NC_000004.10:g.110890213A= NCBI36
NG_007569.1:g.57378T= , LRG_48:g.57378T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695844.1:n.1120-6T=
ENST00000695845.1:n.1119-6T=
ENST00000695846.1:n.965-6T=
ENST00000394634.7:c.941-6T= MANE Select ENSP00000378130.2:n.941-6T=
ENST00000394635.8:c.965-6T= ENSP00000378131.3:n.965-6T=
ENST00000645635.1:c.941-6T= ENSP00000493607.1:n.941-6T=
ENST00000394634.6:c.941-6T= ENSP00000378130.2:n.941-6T=
ENST00000394635.7:c.965-6T= ENSP00000378131.3:n.965-6T=
ENST00000504853.3:n.1358-6T=
ENST00000512148.5:c.920-6T= ENSP00000427438.1:n.920-6T=
ENST00000618244.4:c.941-6T= ENSP00000483416.1:n.941-6T=
NM_000204.3:c.941-6T= , LRG_48t1:c.941-6T= NP_000195.2:n.941-6T=
XM_005262975.1:c.965-6T= XP_005263032.1:n.965-6T=
XM_005262976.1:c.920-6T= XP_005263033.1:n.920-6T=
XM_006714209.1:c.962-6T= XP_006714272.1:n.962-6T=
XM_006714210.2:c.965-6T= XP_006714273.1:n.965-6T=
XM_011531920.1:c.965-6T= XP_011530222.1:n.965-6T=
NM_000204.4:c.941-6T= NP_000195.2:n.941-6T=
NM_001318057.1:c.965-6T= NP_001304986.1:n.965-6T=
NM_001331035.1:c.920-6T= NP_001317964.1:n.920-6T=
XM_006714210.4:c.965-6T= XP_006714273.1:n.965-6T=
XM_011531920.2:c.965-6T= XP_011530222.1:n.965-6T=
XM_017008164.2:c.941-6T= XP_016863653.1:n.941-6T=
XM_017008165.2:c.920-6T= XP_016863654.1:n.920-6T=
XM_017008166.2:c.941-6T= XP_016863655.1:n.941-6T=
NM_001318057.2:c.965-6T= NP_001304986.2:n.965-6T=
NM_001331035.2:c.920-6T= NP_001317964.1:n.920-6T=
NM_001375278.1:c.965-6T= NP_001362207.1:n.965-6T=
NM_001375279.1:c.941-6T= NP_001362208.1:n.941-6T=
NM_001375280.1:c.920-6T= NP_001362209.1:n.920-6T=
NM_001375281.1:c.941-6T= NP_001362210.1:n.941-6T=
NM_001375282.1:c.920-6T= NP_001362211.1:n.920-6T=
NM_001375283.1:c.884-6T= NP_001362212.1:n.884-6T=
NM_001375284.1:c.332-6T= NP_001362213.1:n.332-6T=
NR_164671.1:n.969-6T=
NR_164672.1:n.993-6T=
NR_164673.1:n.969-6T=
NM_000204.5:c.941-6T= MANE Select NP_000195.3:n.941-6T=