Canonical Allele Identifier: CA357854701

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110662246C>A (hg19) ; chr4:g.109741090C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741090C>A , CM000666.2:g.109741090C>A	GRCh38
NC_000004.11:g.110662246C>A , CM000666.1:g.110662246C>A	GRCh37
NC_000004.10:g.110881695C>A	NCBI36
NG_007569.1:g.65896G>T , LRG_48:g.65896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1401G>T
ENST00000695845.1:n.1712+1401G>T
ENST00000695846.1:n.1579G>T
ENST00000394634.7:c.1555G>T MANE Select	ENSP00000378130.2:p.Asp519Tyr
ENST00000394635.8:c.1579G>T	ENSP00000378131.3:p.Asp527Tyr
ENST00000645635.1:c.1534+1401G>T	ENSP00000493607.1:n.1534+1401G>T
ENST00000394634.6:c.1555G>T	ENSP00000378130.2:p.Asp519Tyr
ENST00000394635.7:c.1579G>T	ENSP00000378131.3:p.Asp527Tyr
ENST00000504853.3:n.1972G>T
ENST00000512148.5:c.1534G>T	ENSP00000427438.1:p.Asp512Tyr
ENST00000618244.4:c.1045-285G>T	ENSP00000483416.1:n.1045-285G>T
NM_000204.3:c.1555G>T , LRG_48t1:c.1555G>T	NP_000195.2:p.Asp519Tyr
XM_005262975.1:c.1579G>T	XP_005263032.1:p.Asp527Tyr
XM_005262976.1:c.1534G>T	XP_005263033.1:p.Asp512Tyr
XM_006714209.1:c.1576G>T	XP_006714272.1:p.Asp526Tyr
XM_011531920.1:c.1558+1401G>T	XP_011530222.1:n.1558+1401G>T
NM_000204.4:c.1555G>T	NP_000195.2:p.Asp519Tyr
NM_001318057.1:c.1579G>T	NP_001304986.1:p.Asp527Tyr
NM_001331035.1:c.1534G>T	NP_001317964.1:p.Asp512Tyr
XM_011531920.2:c.1558+1401G>T	XP_011530222.1:n.1558+1401G>T
XM_017008164.2:c.1534+1401G>T	XP_016863653.1:n.1534+1401G>T
XM_017008165.2:c.1513+1401G>T	XP_016863654.1:n.1513+1401G>T
XM_017008166.2:c.1534+1401G>T	XP_016863655.1:n.1534+1401G>T
NM_001318057.2:c.1579G>T	NP_001304986.2:p.Asp527Tyr
NM_001331035.2:c.1534G>T	NP_001317964.1:p.Asp512Tyr
NM_001375278.1:c.1558+1401G>T	NP_001362207.1:n.1558+1401G>T
NM_001375279.1:c.1534+1401G>T	NP_001362208.1:n.1534+1401G>T
NM_001375280.1:c.1513+1401G>T	NP_001362209.1:n.1513+1401G>T
NM_001375281.1:c.1534+1401G>T	NP_001362210.1:n.1534+1401G>T
NM_001375282.1:c.1513+1401G>T	NP_001362211.1:n.1513+1401G>T
NM_001375283.1:c.1498G>T	NP_001362212.1:p.Asp500Tyr
NM_001375284.1:c.946G>T	NP_001362213.1:p.Asp316Tyr
NR_164671.1:n.1302G>T
NR_164672.1:n.1605G>T
NR_164673.1:n.1579G>T
NM_000204.5:c.1555G>T MANE Select	NP_000195.3:p.Asp519Tyr