Canonical Allele Identifier: CA1484705065

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741012T= , CM000666.2:g.109741012T=	GRCh38
NC_000004.11:g.110662168T= , CM000666.1:g.110662168T=	GRCh37
NC_000004.10:g.110881617T=	NCBI36
NG_007569.1:g.65974A= , LRG_48:g.65974A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1479A=
ENST00000695845.1:n.1712+1479A=
ENST00000695846.1:n.1657A=
ENST00000394634.7:c.1633A= MANE Select	ENSP00000378130.2:p.Ser545=
ENST00000394635.8:c.1657A=	ENSP00000378131.3:p.Ser553=
ENST00000645635.1:c.1534+1479A=	ENSP00000493607.1:n.1534+1479A=
ENST00000394634.6:c.1633A=	ENSP00000378130.2:p.Ser545=
ENST00000394635.7:c.1657A=	ENSP00000378131.3:p.Ser553=
ENST00000504853.3:n.2050A=
ENST00000512148.5:c.1612A=	ENSP00000427438.1:p.Ser538=
ENST00000618244.4:c.1045-207A=	ENSP00000483416.1:n.1045-207A=
NM_000204.3:c.1633A= , LRG_48t1:c.1633A=	NP_000195.2:p.Ser545=
XM_005262975.1:c.1657A=	XP_005263032.1:p.Ser553=
XM_005262976.1:c.1612A=	XP_005263033.1:p.Ser538=
XM_006714209.1:c.1654A=	XP_006714272.1:p.Ser552=
XM_011531920.1:c.1558+1479A=	XP_011530222.1:n.1558+1479A=
NM_000204.4:c.1633A=	NP_000195.2:p.Ser545=
NM_001318057.1:c.1657A=	NP_001304986.1:p.Ser553=
NM_001331035.1:c.1612A=	NP_001317964.1:p.Ser538=
XM_011531920.2:c.1558+1479A=	XP_011530222.1:n.1558+1479A=
XM_017008164.2:c.1534+1479A=	XP_016863653.1:n.1534+1479A=
XM_017008165.2:c.1513+1479A=	XP_016863654.1:n.1513+1479A=
XM_017008166.2:c.1534+1479A=	XP_016863655.1:n.1534+1479A=
NM_001318057.2:c.1657A=	NP_001304986.2:p.Ser553=
NM_001331035.2:c.1612A=	NP_001317964.1:p.Ser538=
NM_001375278.1:c.1558+1479A=	NP_001362207.1:n.1558+1479A=
NM_001375279.1:c.1534+1479A=	NP_001362208.1:n.1534+1479A=
NM_001375280.1:c.1513+1479A=	NP_001362209.1:n.1513+1479A=
NM_001375281.1:c.1534+1479A=	NP_001362210.1:n.1534+1479A=
NM_001375282.1:c.1513+1479A=	NP_001362211.1:n.1513+1479A=
NM_001375283.1:c.1576A=	NP_001362212.1:p.Ser526=
NM_001375284.1:c.1024A=	NP_001362213.1:p.Ser342=
NR_164671.1:n.1380A=
NR_164672.1:n.1683A=
NR_164673.1:n.1657A=
NM_000204.5:c.1633A= MANE Select	NP_000195.3:p.Ser545=