Canonical Allele Identifier: CA103695385
Gene: CFI HGNC NCBI

Linked Data

dbSNP Id: rs112534524

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109760371C>G , CM000666.2:g.109760371C>G GRCh38
NC_000004.11:g.110681527C>G , CM000666.1:g.110681527C>G GRCh37
NC_000004.10:g.110900976C>G NCBI36
NG_007569.1:g.46615G>C , LRG_48:g.46615G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695844.1:n.961G>C
ENST00000695845.1:n.960G>C
ENST00000695846.1:n.782G>C
ENST00000394634.7:c.782G>C MANE Select ENSP00000378130.2:p.Gly261Ala
ENST00000394635.8:c.782G>C ENSP00000378131.3:p.Gly261Ala
ENST00000645635.1:c.782G>C ENSP00000493607.1:p.Gly261Ala
ENST00000394634.6:c.782G>C ENSP00000378130.2:p.Gly261Ala
ENST00000394635.7:c.782G>C ENSP00000378131.3:p.Gly261Ala
ENST00000504853.3:n.1199G>C
ENST00000512148.5:c.782G>C ENSP00000427438.1:p.Gly261Ala
ENST00000618244.4:c.782G>C ENSP00000483416.1:p.Gly261Ala
NM_000204.3:c.782G>C , LRG_48t1:c.782G>C NP_000195.2:p.Gly261Ala
XM_005262975.1:c.782G>C XP_005263032.1:p.Gly261Ala
XM_005262976.1:c.782G>C XP_005263033.1:p.Gly261Ala
XM_006714209.1:c.782G>C XP_006714272.1:p.Gly261Ala
XM_006714210.2:c.782G>C XP_006714273.1:p.Gly261Ala
XM_011531920.1:c.782G>C XP_011530222.1:p.Gly261Ala
NM_000204.4:c.782G>C NP_000195.2:p.Gly261Ala
NM_001318057.1:c.782G>C NP_001304986.1:p.Gly261Ala
NM_001331035.1:c.782G>C NP_001317964.1:p.Gly261Ala
XM_006714210.4:c.782G>C XP_006714273.1:p.Gly261Ala
XM_011531920.2:c.782G>C XP_011530222.1:p.Gly261Ala
XM_017008164.2:c.782G>C XP_016863653.1:p.Gly261Ala
XM_017008165.2:c.782G>C XP_016863654.1:p.Gly261Ala
XM_017008166.2:c.782G>C XP_016863655.1:p.Gly261Ala
NM_001318057.2:c.782G>C NP_001304986.2:p.Gly261Ala
NM_001331035.2:c.782G>C NP_001317964.1:p.Gly261Ala
NM_001375278.1:c.782G>C NP_001362207.1:p.Gly261Ala
NM_001375279.1:c.782G>C NP_001362208.1:p.Gly261Ala
NM_001375280.1:c.782G>C NP_001362209.1:p.Gly261Ala
NM_001375281.1:c.782G>C NP_001362210.1:p.Gly261Ala
NM_001375282.1:c.782G>C NP_001362211.1:p.Gly261Ala
NM_001375283.1:c.782G>C NP_001362212.1:p.Gly261Ala
NM_001375284.1:c.173G>C NP_001362213.1:p.Gly58Ala
NR_164671.1:n.810G>C
NR_164672.1:n.810G>C
NR_164673.1:n.810G>C
NM_000204.5:c.782G>C MANE Select NP_000195.3:p.Gly261Ala