Canonical Allele Identifier: CA1484704621

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740697T= , CM000666.2:g.109740697T=	GRCh38
NC_000004.11:g.110661853T= , CM000666.1:g.110661853T=	GRCh37
NC_000004.10:g.110881302T=	NCBI36
NG_007569.1:g.66289A= , LRG_48:g.66289A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1794A=
ENST00000695845.1:n.1712+1794A=
ENST00000394634.7:c.*196A= MANE Select	ENSP00000378130.2:n.*196A=
ENST00000394635.8:c.*196A=	ENSP00000378131.3:n.*196A=
ENST00000645635.1:c.1534+1794A=	ENSP00000493607.1:n.1534+1794A=
ENST00000394634.6:c.*196A=	ENSP00000378130.2:n.*196A=
ENST00000394635.7:c.*196A=	ENSP00000378131.3:n.*196A=
ENST00000504853.3:n.2365A=
NM_000204.3:c.*196A= , LRG_48t1:c.*196A=	NP_000195.2:n.*196A=
XM_005262975.1:c.*196A=	XP_005263032.1:n.*196A=
XM_005262976.1:c.*196A=	XP_005263033.1:n.*196A=
XM_006714209.1:c.*196A=	XP_006714272.1:n.*196A=
XM_011531920.1:c.1558+1794A=	XP_011530222.1:n.1558+1794A=
NM_000204.4:c.*196A=	NP_000195.2:n.*196A=
NM_001318057.1:c.*196A=	NP_001304986.1:n.*196A=
NM_001331035.1:c.*196A=	NP_001317964.1:n.*196A=
XM_011531920.2:c.1558+1794A=	XP_011530222.1:n.1558+1794A=
XM_017008164.2:c.1534+1794A=	XP_016863653.1:n.1534+1794A=
XM_017008165.2:c.1513+1794A=	XP_016863654.1:n.1513+1794A=
XM_017008166.2:c.1534+1794A=	XP_016863655.1:n.1534+1794A=
NM_001318057.2:c.*196A=	NP_001304986.2:n.*196A=
NM_001331035.2:c.*196A=	NP_001317964.1:n.*196A=
NM_001375278.1:c.1558+1794A=	NP_001362207.1:n.1558+1794A=
NM_001375279.1:c.1534+1794A=	NP_001362208.1:n.1534+1794A=
NM_001375280.1:c.1513+1794A=	NP_001362209.1:n.1513+1794A=
NM_001375281.1:c.1534+1794A=	NP_001362210.1:n.1534+1794A=
NM_001375282.1:c.1513+1794A=	NP_001362211.1:n.1513+1794A=
NM_001375283.1:c.*196A=	NP_001362212.1:n.*196A=
NM_001375284.1:c.*196A=	NP_001362213.1:n.*196A=
NR_164671.1:n.1695A=
NR_164672.1:n.1998A=
NR_164673.1:n.1972A=
NM_000204.5:c.*196A= MANE Select	NP_000195.3:n.*196A=