Canonical Allele Identifier: CA357859312

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110670757T>A (hg19) ; chr4:g.109749601T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109749601T>A , CM000666.2:g.109749601T>A	GRCh38
NC_000004.11:g.110670757T>A , CM000666.1:g.110670757T>A	GRCh37
NC_000004.10:g.110890206T>A	NCBI36
NG_007569.1:g.57385A>T , LRG_48:g.57385A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695844.1:n.1121A>T
ENST00000695845.1:n.1120A>T
ENST00000695846.1:n.966A>T
ENST00000394634.7:c.942A>T MANE Select	ENSP00000378130.2:p.Glu314Asp
ENST00000394635.8:c.966A>T	ENSP00000378131.3:p.Glu322Asp
ENST00000645635.1:c.942A>T	ENSP00000493607.1:p.Glu314Asp
ENST00000394634.6:c.942A>T	ENSP00000378130.2:p.Glu314Asp
ENST00000394635.7:c.966A>T	ENSP00000378131.3:p.Glu322Asp
ENST00000504853.3:n.1359A>T
ENST00000512148.5:c.921A>T	ENSP00000427438.1:p.Glu307Asp
ENST00000618244.4:c.942A>T	ENSP00000483416.1:p.Glu314Asp
NM_000204.3:c.942A>T , LRG_48t1:c.942A>T	NP_000195.2:p.Glu314Asp
XM_005262975.1:c.966A>T	XP_005263032.1:p.Glu322Asp
XM_005262976.1:c.921A>T	XP_005263033.1:p.Glu307Asp
XM_006714209.1:c.963A>T	XP_006714272.1:p.Glu321Asp
XM_006714210.2:c.966A>T	XP_006714273.1:p.Glu322Asp
XM_011531920.1:c.966A>T	XP_011530222.1:p.Glu322Asp
NM_000204.4:c.942A>T	NP_000195.2:p.Glu314Asp
NM_001318057.1:c.966A>T	NP_001304986.1:p.Glu322Asp
NM_001331035.1:c.921A>T	NP_001317964.1:p.Glu307Asp
XM_006714210.4:c.966A>T	XP_006714273.1:p.Glu322Asp
XM_011531920.2:c.966A>T	XP_011530222.1:p.Glu322Asp
XM_017008164.2:c.942A>T	XP_016863653.1:p.Glu314Asp
XM_017008165.2:c.921A>T	XP_016863654.1:p.Glu307Asp
XM_017008166.2:c.942A>T	XP_016863655.1:p.Glu314Asp
NM_001318057.2:c.966A>T	NP_001304986.2:p.Glu322Asp
NM_001331035.2:c.921A>T	NP_001317964.1:p.Glu307Asp
NM_001375278.1:c.966A>T	NP_001362207.1:p.Glu322Asp
NM_001375279.1:c.942A>T	NP_001362208.1:p.Glu314Asp
NM_001375280.1:c.921A>T	NP_001362209.1:p.Glu307Asp
NM_001375281.1:c.942A>T	NP_001362210.1:p.Glu314Asp
NM_001375282.1:c.921A>T	NP_001362211.1:p.Glu307Asp
NM_001375283.1:c.885A>T	NP_001362212.1:p.Glu295Asp
NM_001375284.1:c.333A>T	NP_001362213.1:p.Glu111Asp
NR_164671.1:n.970A>T
NR_164672.1:n.994A>T
NR_164673.1:n.970A>T
NM_000204.5:c.942A>T MANE Select	NP_000195.3:p.Glu314Asp