Canonical Allele Identifier: CA357854403

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110662139C>A (hg19) ; chr4:g.109740983C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740983C>A , CM000666.2:g.109740983C>A	GRCh38
NC_000004.11:g.110662139C>A , CM000666.1:g.110662139C>A	GRCh37
NC_000004.10:g.110881588C>A	NCBI36
NG_007569.1:g.66003G>T , LRG_48:g.66003G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1508G>T
ENST00000695845.1:n.1712+1508G>T
ENST00000695846.1:n.1686G>T
ENST00000394634.7:c.1662G>T MANE Select	ENSP00000378130.2:p.Glu554Asp
ENST00000394635.8:c.1686G>T	ENSP00000378131.3:p.Glu562Asp
ENST00000645635.1:c.1534+1508G>T	ENSP00000493607.1:n.1534+1508G>T
ENST00000394634.6:c.1662G>T	ENSP00000378130.2:p.Glu554Asp
ENST00000394635.7:c.1686G>T	ENSP00000378131.3:p.Glu562Asp
ENST00000504853.3:n.2079G>T
ENST00000512148.5:c.1641G>T	ENSP00000427438.1:p.Glu547Asp
ENST00000618244.4:c.1045-178G>T	ENSP00000483416.1:n.1045-178G>T
NM_000204.3:c.1662G>T , LRG_48t1:c.1662G>T	NP_000195.2:p.Glu554Asp
XM_005262975.1:c.1686G>T	XP_005263032.1:p.Glu562Asp
XM_005262976.1:c.1641G>T	XP_005263033.1:p.Glu547Asp
XM_006714209.1:c.1683G>T	XP_006714272.1:p.Glu561Asp
XM_011531920.1:c.1558+1508G>T	XP_011530222.1:n.1558+1508G>T
NM_000204.4:c.1662G>T	NP_000195.2:p.Glu554Asp
NM_001318057.1:c.1686G>T	NP_001304986.1:p.Glu562Asp
NM_001331035.1:c.1641G>T	NP_001317964.1:p.Glu547Asp
XM_011531920.2:c.1558+1508G>T	XP_011530222.1:n.1558+1508G>T
XM_017008164.2:c.1534+1508G>T	XP_016863653.1:n.1534+1508G>T
XM_017008165.2:c.1513+1508G>T	XP_016863654.1:n.1513+1508G>T
XM_017008166.2:c.1534+1508G>T	XP_016863655.1:n.1534+1508G>T
NM_001318057.2:c.1686G>T	NP_001304986.2:p.Glu562Asp
NM_001331035.2:c.1641G>T	NP_001317964.1:p.Glu547Asp
NM_001375278.1:c.1558+1508G>T	NP_001362207.1:n.1558+1508G>T
NM_001375279.1:c.1534+1508G>T	NP_001362208.1:n.1534+1508G>T
NM_001375280.1:c.1513+1508G>T	NP_001362209.1:n.1513+1508G>T
NM_001375281.1:c.1534+1508G>T	NP_001362210.1:n.1534+1508G>T
NM_001375282.1:c.1513+1508G>T	NP_001362211.1:n.1513+1508G>T
NM_001375283.1:c.1605G>T	NP_001362212.1:p.Glu535Asp
NM_001375284.1:c.1053G>T	NP_001362213.1:p.Glu351Asp
NR_164671.1:n.1409G>T
NR_164672.1:n.1712G>T
NR_164673.1:n.1686G>T
NM_000204.5:c.1662G>T MANE Select	NP_000195.3:p.Glu554Asp