Canonical Allele Identifier: CA440583601

Gene: CFI

Linked Data

• gnomAD v4: 4-109746256-A-G
• MyVariant Identifiers: chr4:g.110667412A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109746256A>G , CM000666.2:g.109746256A>G	GRCh38
NC_000004.11:g.110667412A>G , CM000666.1:g.110667412A>G	GRCh37
NC_000004.10:g.110886861A>G	NCBI36
NG_007569.1:g.60730T>C , LRG_48:g.60730T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695844.1:n.1574T>C
ENST00000695845.1:n.1573T>C
ENST00000695846.1:n.1419T>C
ENST00000394634.7:c.1395T>C MANE Select	ENSP00000378130.2:p.Asp465=
ENST00000394635.8:c.1419T>C	ENSP00000378131.3:p.Asp473=
ENST00000645635.1:c.1395T>C	ENSP00000493607.1:p.Asp465=
ENST00000394634.6:c.1395T>C	ENSP00000378130.2:p.Asp465=
ENST00000394635.7:c.1419T>C	ENSP00000378131.3:p.Asp473=
ENST00000504853.3:n.1812T>C
ENST00000512148.5:c.1374T>C	ENSP00000427438.1:p.Asp458=
ENST00000515512.1:n.37T>C
ENST00000618244.4:c.1044+3243T>C	ENSP00000483416.1:n.1044+3243T>C
NM_000204.3:c.1395T>C , LRG_48t1:c.1395T>C	NP_000195.2:p.Asp465=
XM_005262975.1:c.1419T>C	XP_005263032.1:p.Asp473=
XM_005262976.1:c.1374T>C	XP_005263033.1:p.Asp458=
XM_006714209.1:c.1416T>C	XP_006714272.1:p.Asp472=
XM_006714210.2:c.1419T>C	XP_006714273.1:p.Asp473=
XM_011531920.1:c.1419T>C	XP_011530222.1:p.Asp473=
NM_000204.4:c.1395T>C	NP_000195.2:p.Asp465=
NM_001318057.1:c.1419T>C	NP_001304986.1:p.Asp473=
NM_001331035.1:c.1374T>C	NP_001317964.1:p.Asp458=
XM_006714210.4:c.1419T>C	XP_006714273.1:p.Asp473=
XM_011531920.2:c.1419T>C	XP_011530222.1:p.Asp473=
XM_017008164.2:c.1395T>C	XP_016863653.1:p.Asp465=
XM_017008165.2:c.1374T>C	XP_016863654.1:p.Asp458=
XM_017008166.2:c.1395T>C	XP_016863655.1:p.Asp465=
NM_001318057.2:c.1419T>C	NP_001304986.2:p.Asp473=
NM_001331035.2:c.1374T>C	NP_001317964.1:p.Asp458=
NM_001375278.1:c.1419T>C	NP_001362207.1:p.Asp473=
NM_001375279.1:c.1395T>C	NP_001362208.1:p.Asp465=
NM_001375280.1:c.1374T>C	NP_001362209.1:p.Asp458=
NM_001375281.1:c.1395T>C	NP_001362210.1:p.Asp465=
NM_001375282.1:c.1374T>C	NP_001362211.1:p.Asp458=
NM_001375283.1:c.1338T>C	NP_001362212.1:p.Asp446=
NM_001375284.1:c.786T>C	NP_001362213.1:p.Asp262=
NR_164671.1:n.1176+2962T>C
NR_164672.1:n.1445T>C
NR_164673.1:n.1419T>C
NM_000204.5:c.1395T>C MANE Select	NP_000195.3:p.Asp465=