Canonical Allele Identifier: CA1484704889

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740908A= , CM000666.2:g.109740908A=	GRCh38
NC_000004.11:g.110662064A= , CM000666.1:g.110662064A=	GRCh37
NC_000004.10:g.110881513A=	NCBI36
NG_007569.1:g.66078T= , LRG_48:g.66078T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1583T=
ENST00000695845.1:n.1712+1583T=
ENST00000695846.1:n.1761T=
ENST00000394634.7:c.1737T= MANE Select	ENSP00000378130.2:p.Ser579=
ENST00000394635.8:c.1761T=	ENSP00000378131.3:p.Ser587=
ENST00000645635.1:c.1534+1583T=	ENSP00000493607.1:n.1534+1583T=
ENST00000394634.6:c.1737T=	ENSP00000378130.2:p.Ser579=
ENST00000394635.7:c.1761T=	ENSP00000378131.3:p.Ser587=
ENST00000504853.3:n.2154T=
ENST00000512148.5:c.1716T=	ENSP00000427438.1:p.Ser572=
ENST00000618244.4:c.1045-103T=	ENSP00000483416.1:n.1045-103T=
NM_000204.3:c.1737T= , LRG_48t1:c.1737T=	NP_000195.2:p.Ser579=
XM_005262975.1:c.1761T=	XP_005263032.1:p.Ser587=
XM_005262976.1:c.1716T=	XP_005263033.1:p.Ser572=
XM_006714209.1:c.1758T=	XP_006714272.1:p.Ser586=
XM_011531920.1:c.1558+1583T=	XP_011530222.1:n.1558+1583T=
NM_000204.4:c.1737T=	NP_000195.2:p.Ser579=
NM_001318057.1:c.1761T=	NP_001304986.1:p.Ser587=
NM_001331035.1:c.1716T=	NP_001317964.1:p.Ser572=
XM_011531920.2:c.1558+1583T=	XP_011530222.1:n.1558+1583T=
XM_017008164.2:c.1534+1583T=	XP_016863653.1:n.1534+1583T=
XM_017008165.2:c.1513+1583T=	XP_016863654.1:n.1513+1583T=
XM_017008166.2:c.1534+1583T=	XP_016863655.1:n.1534+1583T=
NM_001318057.2:c.1761T=	NP_001304986.2:p.Ser587=
NM_001331035.2:c.1716T=	NP_001317964.1:p.Ser572=
NM_001375278.1:c.1558+1583T=	NP_001362207.1:n.1558+1583T=
NM_001375279.1:c.1534+1583T=	NP_001362208.1:n.1534+1583T=
NM_001375280.1:c.1513+1583T=	NP_001362209.1:n.1513+1583T=
NM_001375281.1:c.1534+1583T=	NP_001362210.1:n.1534+1583T=
NM_001375282.1:c.1513+1583T=	NP_001362211.1:n.1513+1583T=
NM_001375283.1:c.1680T=	NP_001362212.1:p.Ser560=
NM_001375284.1:c.1128T=	NP_001362213.1:p.Ser376=
NR_164671.1:n.1484T=
NR_164672.1:n.1787T=
NR_164673.1:n.1761T=
NM_000204.5:c.1737T= MANE Select	NP_000195.3:p.Ser579=