Canonical Allele Identifier: CA357860769
Gene: CFI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109757781A>G , CM000666.2:g.109757781A>G GRCh38
NC_000004.11:g.110678937A>G , CM000666.1:g.110678937A>G GRCh37
NC_000004.10:g.110898386A>G NCBI36
NG_007569.1:g.49205T>C , LRG_48:g.49205T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1065T>C
ENST00000695845.1:n.1064T>C
ENST00000695846.1:n.910T>C
ENST00000394634.7:c.886T>C MANE Select ENSP00000378130.2:p.Phe296Leu
ENST00000394635.8:c.910T>C ENSP00000378131.3:p.Phe304Leu
ENST00000645635.1:c.886T>C ENSP00000493607.1:p.Phe296Leu
ENST00000394634.6:c.886T>C ENSP00000378130.2:p.Phe296Leu
ENST00000394635.7:c.910T>C ENSP00000378131.3:p.Phe304Leu
ENST00000504853.3:n.1303T>C
ENST00000512148.5:c.883+2489T>C ENSP00000427438.1:n.883+2489T>C
ENST00000618244.4:c.886T>C ENSP00000483416.1:p.Phe296Leu
NM_000204.3:c.886T>C , LRG_48t1:c.886T>C NP_000195.2:p.Phe296Leu
XM_005262975.1:c.910T>C XP_005263032.1:p.Phe304Leu
XM_005262976.1:c.883+2489T>C XP_005263033.1:n.883+2489T>C
XM_006714209.1:c.907T>C XP_006714272.1:p.Phe303Leu
XM_006714210.2:c.910T>C XP_006714273.1:p.Phe304Leu
XM_011531920.1:c.910T>C XP_011530222.1:p.Phe304Leu
NM_000204.4:c.886T>C NP_000195.2:p.Phe296Leu
NM_001318057.1:c.910T>C NP_001304986.1:p.Phe304Leu
NM_001331035.1:c.883+2489T>C NP_001317964.1:n.883+2489T>C
XM_006714210.4:c.910T>C XP_006714273.1:p.Phe304Leu
XM_011531920.2:c.910T>C XP_011530222.1:p.Phe304Leu
XM_017008164.2:c.886T>C XP_016863653.1:p.Phe296Leu
XM_017008165.2:c.883+2489T>C XP_016863654.1:n.883+2489T>C
XM_017008166.2:c.886T>C XP_016863655.1:p.Phe296Leu
NM_001318057.2:c.910T>C NP_001304986.2:p.Phe304Leu
NM_001331035.2:c.883+2489T>C NP_001317964.1:n.883+2489T>C
NM_001375278.1:c.910T>C NP_001362207.1:p.Phe304Leu
NM_001375279.1:c.886T>C NP_001362208.1:p.Phe296Leu
NM_001375280.1:c.883+2489T>C NP_001362209.1:n.883+2489T>C
NM_001375281.1:c.886T>C NP_001362210.1:p.Phe296Leu
NM_001375282.1:c.883+2489T>C NP_001362211.1:n.883+2489T>C
NM_001375283.1:c.883+2489T>C NP_001362212.1:n.883+2489T>C
NM_001375284.1:c.277T>C NP_001362213.1:p.Phe93Leu
NR_164671.1:n.914T>C
NR_164672.1:n.938T>C
NR_164673.1:n.914T>C
NM_000204.5:c.886T>C MANE Select NP_000195.3:p.Phe296Leu