Canonical Allele Identifier: CA357856610

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109746254G>C , CM000666.2:g.109746254G>C	GRCh38
NC_000004.11:g.110667410G>C , CM000666.1:g.110667410G>C	GRCh37
NC_000004.10:g.110886859G>C	NCBI36
NG_007569.1:g.60732C>G , LRG_48:g.60732C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1576C>G
ENST00000695845.1:n.1575C>G
ENST00000695846.1:n.1421C>G
ENST00000394634.7:c.1397C>G MANE Select	ENSP00000378130.2:p.Thr466Arg
ENST00000394635.8:c.1421C>G	ENSP00000378131.3:p.Thr474Arg
ENST00000645635.1:c.1397C>G	ENSP00000493607.1:p.Thr466Arg
ENST00000394634.6:c.1397C>G	ENSP00000378130.2:p.Thr466Arg
ENST00000394635.7:c.1421C>G	ENSP00000378131.3:p.Thr474Arg
ENST00000504853.3:n.1814C>G
ENST00000512148.5:c.1376C>G	ENSP00000427438.1:p.Thr459Arg
ENST00000515512.1:n.39C>G
ENST00000618244.4:c.1044+3245C>G	ENSP00000483416.1:n.1044+3245C>G
NM_000204.3:c.1397C>G , LRG_48t1:c.1397C>G	NP_000195.2:p.Thr466Arg
XM_005262975.1:c.1421C>G	XP_005263032.1:p.Thr474Arg
XM_005262976.1:c.1376C>G	XP_005263033.1:p.Thr459Arg
XM_006714209.1:c.1418C>G	XP_006714272.1:p.Thr473Arg
XM_006714210.2:c.1421C>G	XP_006714273.1:p.Thr474Arg
XM_011531920.1:c.1421C>G	XP_011530222.1:p.Thr474Arg
NM_000204.4:c.1397C>G	NP_000195.2:p.Thr466Arg
NM_001318057.1:c.1421C>G	NP_001304986.1:p.Thr474Arg
NM_001331035.1:c.1376C>G	NP_001317964.1:p.Thr459Arg
XM_006714210.4:c.1421C>G	XP_006714273.1:p.Thr474Arg
XM_011531920.2:c.1421C>G	XP_011530222.1:p.Thr474Arg
XM_017008164.2:c.1397C>G	XP_016863653.1:p.Thr466Arg
XM_017008165.2:c.1376C>G	XP_016863654.1:p.Thr459Arg
XM_017008166.2:c.1397C>G	XP_016863655.1:p.Thr466Arg
NM_001318057.2:c.1421C>G	NP_001304986.2:p.Thr474Arg
NM_001331035.2:c.1376C>G	NP_001317964.1:p.Thr459Arg
NM_001375278.1:c.1421C>G	NP_001362207.1:p.Thr474Arg
NM_001375279.1:c.1397C>G	NP_001362208.1:p.Thr466Arg
NM_001375280.1:c.1376C>G	NP_001362209.1:p.Thr459Arg
NM_001375281.1:c.1397C>G	NP_001362210.1:p.Thr466Arg
NM_001375282.1:c.1376C>G	NP_001362211.1:p.Thr459Arg
NM_001375283.1:c.1340C>G	NP_001362212.1:p.Thr447Arg
NM_001375284.1:c.788C>G	NP_001362213.1:p.Thr263Arg
NR_164671.1:n.1176+2964C>G
NR_164672.1:n.1447C>G
NR_164673.1:n.1421C>G
NM_000204.5:c.1397C>G MANE Select	NP_000195.3:p.Thr466Arg