Canonical Allele Identifier: CA1484709942
Gene: CFI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109744989_109745006delinsTCAGACATACCACAAATC , CM000666.2:g.109744989_109745006delinsTCAGACATACCACAAATC GRCh38
NC_000004.11:g.110666145_110666162delinsTCAGACATACCACAAATC , CM000666.1:g.110666145_110666162delinsTCAGACATACCACAAATC GRCh37
NC_000004.10:g.110885594_110885611delinsTCAGACATACCACAAATC NCBI36
NG_007569.1:g.61980_61997delinsGATTTGTGGTATGTCTGA , LRG_48:g.61980_61997delinsGATTTGTGGTATGTCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695844.1:n.1608+1216_1608+1233delinsGATTTGTGGTATGTCTGA
ENST00000695845.1:n.1607+1216_1607+1233delinsGATTTGTGGTATGTCTGA
ENST00000695846.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
ENST00000394634.7:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA MANE Select ENSP00000378130.2:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCT...
ENST00000394635.8:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA ENSP00000378131.3:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCT...
ENST00000645635.1:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA ENSP00000493607.1:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCT...
ENST00000394634.6:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA ENSP00000378130.2:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCT...
ENST00000394635.7:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA ENSP00000378131.3:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCT...
ENST00000504853.3:n.1846+1216_1846+1233delinsGATTTGTGGTATGTCTGA
ENST00000512148.5:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA ENSP00000427438.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCT...
ENST00000515512.1:n.71+1216_71+1233delinsGATTTGTGGTATGTCTGA
ENST00000618244.4:c.1045-4201_1045-4184delinsGATTTGTGGTATGTCTGA ENSP00000483416.1:n.1045-4201_1045-4184delinsGATTTGTGGTATGTCT...
NM_000204.3:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA , LRG_48t1:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA NP_000195.2:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA
XM_005262975.1:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA XP_005263032.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
XM_005262976.1:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA XP_005263033.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA
XM_006714209.1:c.1450+1216_1450+1233delinsGATTTGTGGTATGTCTGA XP_006714272.1:n.1450+1216_1450+1233delinsGATTTGTGGTATGTCTGA
XM_006714210.2:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA XP_006714273.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
XM_011531920.1:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA XP_011530222.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
NM_000204.4:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA NP_000195.2:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA
NM_001318057.1:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA NP_001304986.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
NM_001331035.1:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA NP_001317964.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA
XM_006714210.4:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA XP_006714273.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
XM_011531920.2:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA XP_011530222.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
XM_017008164.2:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA XP_016863653.1:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA
XM_017008165.2:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA XP_016863654.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA
XM_017008166.2:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA XP_016863655.1:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA
NM_001318057.2:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA NP_001304986.2:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
NM_001331035.2:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA NP_001317964.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA
NM_001375278.1:c.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA NP_001362207.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
NM_001375279.1:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA NP_001362208.1:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA
NM_001375280.1:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA NP_001362209.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA
NM_001375281.1:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA NP_001362210.1:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA
NM_001375282.1:c.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA NP_001362211.1:n.1408+1216_1408+1233delinsGATTTGTGGTATGTCTGA
NM_001375283.1:c.1372+1216_1372+1233delinsGATTTGTGGTATGTCTGA NP_001362212.1:n.1372+1216_1372+1233delinsGATTTGTGGTATGTCTGA
NM_001375284.1:c.820+1216_820+1233delinsGATTTGTGGTATGTCTGA NP_001362213.1:n.820+1216_820+1233delinsGATTTGTGGTATGTCTGA
NR_164671.1:n.1177-2411_1177-2394delinsGATTTGTGGTATGTCTGA
NR_164672.1:n.1479+1216_1479+1233delinsGATTTGTGGTATGTCTGA
NR_164673.1:n.1453+1216_1453+1233delinsGATTTGTGGTATGTCTGA
NM_000204.5:c.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA MANE Select NP_000195.3:n.1429+1216_1429+1233delinsGATTTGTGGTATGTCTGA