Canonical Allele Identifier: CA357860734
Gene: CFI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109757764T>A , CM000666.2:g.109757764T>A GRCh38
NC_000004.11:g.110678920T>A , CM000666.1:g.110678920T>A GRCh37
NC_000004.10:g.110898369T>A NCBI36
NG_007569.1:g.49222A>T , LRG_48:g.49222A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1082A>T
ENST00000695845.1:n.1081A>T
ENST00000695846.1:n.927A>T
ENST00000394634.7:c.903A>T MANE Select ENSP00000378130.2:p.Gln301His
ENST00000394635.8:c.927A>T ENSP00000378131.3:p.Gln309His
ENST00000645635.1:c.903A>T ENSP00000493607.1:p.Gln301His
ENST00000394634.6:c.903A>T ENSP00000378130.2:p.Gln301His
ENST00000394635.7:c.927A>T ENSP00000378131.3:p.Gln309His
ENST00000504853.3:n.1320A>T
ENST00000512148.5:c.883+2506A>T ENSP00000427438.1:n.883+2506A>T
ENST00000618244.4:c.903A>T ENSP00000483416.1:p.Gln301His
NM_000204.3:c.903A>T , LRG_48t1:c.903A>T NP_000195.2:p.Gln301His
XM_005262975.1:c.927A>T XP_005263032.1:p.Gln309His
XM_005262976.1:c.883+2506A>T XP_005263033.1:n.883+2506A>T
XM_006714209.1:c.924A>T XP_006714272.1:p.Gln308His
XM_006714210.2:c.927A>T XP_006714273.1:p.Gln309His
XM_011531920.1:c.927A>T XP_011530222.1:p.Gln309His
NM_000204.4:c.903A>T NP_000195.2:p.Gln301His
NM_001318057.1:c.927A>T NP_001304986.1:p.Gln309His
NM_001331035.1:c.883+2506A>T NP_001317964.1:n.883+2506A>T
XM_006714210.4:c.927A>T XP_006714273.1:p.Gln309His
XM_011531920.2:c.927A>T XP_011530222.1:p.Gln309His
XM_017008164.2:c.903A>T XP_016863653.1:p.Gln301His
XM_017008165.2:c.883+2506A>T XP_016863654.1:n.883+2506A>T
XM_017008166.2:c.903A>T XP_016863655.1:p.Gln301His
NM_001318057.2:c.927A>T NP_001304986.2:p.Gln309His
NM_001331035.2:c.883+2506A>T NP_001317964.1:n.883+2506A>T
NM_001375278.1:c.927A>T NP_001362207.1:p.Gln309His
NM_001375279.1:c.903A>T NP_001362208.1:p.Gln301His
NM_001375280.1:c.883+2506A>T NP_001362209.1:n.883+2506A>T
NM_001375281.1:c.903A>T NP_001362210.1:p.Gln301His
NM_001375282.1:c.883+2506A>T NP_001362211.1:n.883+2506A>T
NM_001375283.1:c.883+2506A>T NP_001362212.1:n.883+2506A>T
NM_001375284.1:c.294A>T NP_001362213.1:p.Gln98His
NR_164671.1:n.931A>T
NR_164672.1:n.955A>T
NR_164673.1:n.931A>T
NM_000204.5:c.903A>T MANE Select NP_000195.3:p.Gln301His