Canonical Allele Identifier: CA1484704612

Gene: CFI

Linked Data

• dbSNP Id: rs1723674758

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740690_109740691insGCTGAGGGATTTCATCAATG , CM000666.2:g.109740690_109740691insGCTGAGGGATTTCATCAATG	GRCh38
NC_000004.11:g.110661846_110661847insGCTGAGGGATTTCATCAATG , CM000666.1:g.110661846_110661847insGCTGAGGGATTTCATCAATG	GRCh37
NC_000004.10:g.110881295_110881296insGCTGAGGGATTTCATCAATG	NCBI36
NG_007569.1:g.66295_66296insCATTGATGAAATCCCTCAGC , LRG_48:g.66295_66296insCATTGATGAAATCCCTCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1800_1713+1801insCATTGATGAAATCCCTCAGC
ENST00000695845.1:n.1712+1800_1712+1801insCATTGATGAAATCCCTCAGC
ENST00000645635.1:c.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC	ENSP00000493607.1:n.1534+1800_1534+1801insCATTGATGAAATCCCTCAG...
XM_011531920.1:c.1558+1800_1558+1801insCATTGATGAAATCCCTCAGC	XP_011530222.1:n.1558+1800_1558+1801insCATTGATGAAATCCCTCAGC
XM_011531920.2:c.1558+1800_1558+1801insCATTGATGAAATCCCTCAGC	XP_011530222.1:n.1558+1800_1558+1801insCATTGATGAAATCCCTCAGC
XM_017008164.2:c.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC	XP_016863653.1:n.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC
XM_017008165.2:c.1513+1800_1513+1801insCATTGATGAAATCCCTCAGC	XP_016863654.1:n.1513+1800_1513+1801insCATTGATGAAATCCCTCAGC
XM_017008166.2:c.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC	XP_016863655.1:n.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC
NM_001375278.1:c.1558+1800_1558+1801insCATTGATGAAATCCCTCAGC	NP_001362207.1:n.1558+1800_1558+1801insCATTGATGAAATCCCTCAGC
NM_001375279.1:c.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC	NP_001362208.1:n.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC
NM_001375280.1:c.1513+1800_1513+1801insCATTGATGAAATCCCTCAGC	NP_001362209.1:n.1513+1800_1513+1801insCATTGATGAAATCCCTCAGC
NM_001375281.1:c.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC	NP_001362210.1:n.1534+1800_1534+1801insCATTGATGAAATCCCTCAGC
NM_001375282.1:c.1513+1800_1513+1801insCATTGATGAAATCCCTCAGC	NP_001362211.1:n.1513+1800_1513+1801insCATTGATGAAATCCCTCAGC