Canonical Allele Identifier: CA2706789609

Gene: CFI

Linked Data

• dbSNP Id: rs2126177821

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740875A>G , CM000666.2:g.109740875A>G	GRCh38
NC_000004.11:g.110662031A>G , CM000666.1:g.110662031A>G	GRCh37
NC_000004.10:g.110881480A>G	NCBI36
NG_007569.1:g.66111T>C , LRG_48:g.66111T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1616T>C
ENST00000695845.1:n.1712+1616T>C
ENST00000695846.1:n.1794T>C
ENST00000394634.7:c.*18T>C MANE Select	ENSP00000378130.2:n.*18T>C
ENST00000394635.8:c.*18T>C	ENSP00000378131.3:n.*18T>C
ENST00000645635.1:c.1534+1616T>C	ENSP00000493607.1:n.1534+1616T>C
ENST00000394634.6:c.*18T>C	ENSP00000378130.2:n.*18T>C
ENST00000394635.7:c.*18T>C	ENSP00000378131.3:n.*18T>C
ENST00000504853.3:n.2187T>C
ENST00000512148.5:c.*18T>C	ENSP00000427438.1:n.*18T>C
ENST00000618244.4:c.1045-70T>C	ENSP00000483416.1:n.1045-70T>C
NM_000204.3:c.*18T>C , LRG_48t1:c.*18T>C	NP_000195.2:n.*18T>C
XM_005262975.1:c.*18T>C	XP_005263032.1:n.*18T>C
XM_005262976.1:c.*18T>C	XP_005263033.1:n.*18T>C
XM_006714209.1:c.*18T>C	XP_006714272.1:n.*18T>C
XM_011531920.1:c.1558+1616T>C	XP_011530222.1:n.1558+1616T>C
NM_000204.4:c.*18T>C	NP_000195.2:n.*18T>C
NM_001318057.1:c.*18T>C	NP_001304986.1:n.*18T>C
NM_001331035.1:c.*18T>C	NP_001317964.1:n.*18T>C
XM_011531920.2:c.1558+1616T>C	XP_011530222.1:n.1558+1616T>C
XM_017008164.2:c.1534+1616T>C	XP_016863653.1:n.1534+1616T>C
XM_017008165.2:c.1513+1616T>C	XP_016863654.1:n.1513+1616T>C
XM_017008166.2:c.1534+1616T>C	XP_016863655.1:n.1534+1616T>C
NM_001318057.2:c.*18T>C	NP_001304986.2:n.*18T>C
NM_001331035.2:c.*18T>C	NP_001317964.1:n.*18T>C
NM_001375278.1:c.1558+1616T>C	NP_001362207.1:n.1558+1616T>C
NM_001375279.1:c.1534+1616T>C	NP_001362208.1:n.1534+1616T>C
NM_001375280.1:c.1513+1616T>C	NP_001362209.1:n.1513+1616T>C
NM_001375281.1:c.1534+1616T>C	NP_001362210.1:n.1534+1616T>C
NM_001375282.1:c.1513+1616T>C	NP_001362211.1:n.1513+1616T>C
NM_001375283.1:c.*18T>C	NP_001362212.1:n.*18T>C
NM_001375284.1:c.*18T>C	NP_001362213.1:n.*18T>C
NR_164671.1:n.1517T>C
NR_164672.1:n.1820T>C
NR_164673.1:n.1794T>C
NM_000204.5:c.*18T>C MANE Select	NP_000195.3:n.*18T>C