Canonical Allele Identifier: CA917275688

Gene: CFI

Linked Data

• dbSNP Id: rs1579161352
• gnomAD v3: 4-109745168-TTCC-T
• gnomAD v4: 4-109745168-TTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109745170_109745172del , CM000666.2:g.109745170_109745172del	GRCh38
NC_000004.11:g.110666326_110666328del , CM000666.1:g.110666326_110666328del	GRCh37
NC_000004.10:g.110885775_110885777del	NCBI36
NG_007569.1:g.61815_61817del , LRG_48:g.61815_61817del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695844.1:n.1608+1051_1608+1053del
ENST00000695845.1:n.1607+1051_1607+1053del
ENST00000695846.1:n.1453+1051_1453+1053del
ENST00000394634.7:c.1429+1051_1429+1053del MANE Select	ENSP00000378130.2:n.1429+1051_1429+1053de...
ENST00000394635.8:c.1453+1051_1453+1053del	ENSP00000378131.3:n.1453+1051_1453+1053de...
ENST00000645635.1:c.1429+1051_1429+1053del	ENSP00000493607.1:n.1429+1051_1429+1053de...
ENST00000394634.6:c.1429+1051_1429+1053del	ENSP00000378130.2:n.1429+1051_1429+1053de...
ENST00000394635.7:c.1453+1051_1453+1053del	ENSP00000378131.3:n.1453+1051_1453+1053de...
ENST00000504853.3:n.1846+1051_1846+1053del
ENST00000512148.5:c.1408+1051_1408+1053del	ENSP00000427438.1:n.1408+1051_1408+1053de...
ENST00000515512.1:n.71+1051_71+1053del
ENST00000618244.4:c.1044+4328_1044+4330del	ENSP00000483416.1:n.1044+4328_1044+4330de...
NM_000204.3:c.1429+1051_1429+1053del , LRG_48t1:c.1429+1051_1429+1053del	NP_000195.2:n.1429+1051_1429+1053del
XM_005262975.1:c.1453+1051_1453+1053del	XP_005263032.1:n.1453+1051_1453+1053del
XM_005262976.1:c.1408+1051_1408+1053del	XP_005263033.1:n.1408+1051_1408+1053del
XM_006714209.1:c.1450+1051_1450+1053del	XP_006714272.1:n.1450+1051_1450+1053del
XM_006714210.2:c.1453+1051_1453+1053del	XP_006714273.1:n.1453+1051_1453+1053del
XM_011531920.1:c.1453+1051_1453+1053del	XP_011530222.1:n.1453+1051_1453+1053del
NM_000204.4:c.1429+1051_1429+1053del	NP_000195.2:n.1429+1051_1429+1053del
NM_001318057.1:c.1453+1051_1453+1053del	NP_001304986.1:n.1453+1051_1453+1053del
NM_001331035.1:c.1408+1051_1408+1053del	NP_001317964.1:n.1408+1051_1408+1053del
XM_006714210.4:c.1453+1051_1453+1053del	XP_006714273.1:n.1453+1051_1453+1053del
XM_011531920.2:c.1453+1051_1453+1053del	XP_011530222.1:n.1453+1051_1453+1053del
XM_017008164.2:c.1429+1051_1429+1053del	XP_016863653.1:n.1429+1051_1429+1053del
XM_017008165.2:c.1408+1051_1408+1053del	XP_016863654.1:n.1408+1051_1408+1053del
XM_017008166.2:c.1429+1051_1429+1053del	XP_016863655.1:n.1429+1051_1429+1053del
NM_001318057.2:c.1453+1051_1453+1053del	NP_001304986.2:n.1453+1051_1453+1053del
NM_001331035.2:c.1408+1051_1408+1053del	NP_001317964.1:n.1408+1051_1408+1053del
NM_001375278.1:c.1453+1051_1453+1053del	NP_001362207.1:n.1453+1051_1453+1053del
NM_001375279.1:c.1429+1051_1429+1053del	NP_001362208.1:n.1429+1051_1429+1053del
NM_001375280.1:c.1408+1051_1408+1053del	NP_001362209.1:n.1408+1051_1408+1053del
NM_001375281.1:c.1429+1051_1429+1053del	NP_001362210.1:n.1429+1051_1429+1053del
NM_001375282.1:c.1408+1051_1408+1053del	NP_001362211.1:n.1408+1051_1408+1053del
NM_001375283.1:c.1372+1051_1372+1053del	NP_001362212.1:n.1372+1051_1372+1053del
NM_001375284.1:c.820+1051_820+1053del	NP_001362213.1:n.820+1051_820+1053del
NR_164671.1:n.1177-2576_1177-2574del
NR_164672.1:n.1479+1051_1479+1053del
NR_164673.1:n.1453+1051_1453+1053del
NM_000204.5:c.1429+1051_1429+1053del MANE Select	NP_000195.3:n.1429+1051_1429+1053del