Canonical Allele Identifier: CA357856592

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110667401A>T (hg19) ; chr4:g.109746245A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109746245A>T , CM000666.2:g.109746245A>T	GRCh38
NC_000004.11:g.110667401A>T , CM000666.1:g.110667401A>T	GRCh37
NC_000004.10:g.110886850A>T	NCBI36
NG_007569.1:g.60741T>A , LRG_48:g.60741T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1585T>A
ENST00000695845.1:n.1584T>A
ENST00000695846.1:n.1430T>A
ENST00000394634.7:c.1406T>A MANE Select	ENSP00000378130.2:p.Val469Asp
ENST00000394635.8:c.1430T>A	ENSP00000378131.3:p.Val477Asp
ENST00000645635.1:c.1406T>A	ENSP00000493607.1:p.Val469Asp
ENST00000394634.6:c.1406T>A	ENSP00000378130.2:p.Val469Asp
ENST00000394635.7:c.1430T>A	ENSP00000378131.3:p.Val477Asp
ENST00000504853.3:n.1823T>A
ENST00000512148.5:c.1385T>A	ENSP00000427438.1:p.Val462Asp
ENST00000515512.1:n.48T>A
ENST00000618244.4:c.1044+3254T>A	ENSP00000483416.1:n.1044+3254T>A
NM_000204.3:c.1406T>A , LRG_48t1:c.1406T>A	NP_000195.2:p.Val469Asp
XM_005262975.1:c.1430T>A	XP_005263032.1:p.Val477Asp
XM_005262976.1:c.1385T>A	XP_005263033.1:p.Val462Asp
XM_006714209.1:c.1427T>A	XP_006714272.1:p.Val476Asp
XM_006714210.2:c.1430T>A	XP_006714273.1:p.Val477Asp
XM_011531920.1:c.1430T>A	XP_011530222.1:p.Val477Asp
NM_000204.4:c.1406T>A	NP_000195.2:p.Val469Asp
NM_001318057.1:c.1430T>A	NP_001304986.1:p.Val477Asp
NM_001331035.1:c.1385T>A	NP_001317964.1:p.Val462Asp
XM_006714210.4:c.1430T>A	XP_006714273.1:p.Val477Asp
XM_011531920.2:c.1430T>A	XP_011530222.1:p.Val477Asp
XM_017008164.2:c.1406T>A	XP_016863653.1:p.Val469Asp
XM_017008165.2:c.1385T>A	XP_016863654.1:p.Val462Asp
XM_017008166.2:c.1406T>A	XP_016863655.1:p.Val469Asp
NM_001318057.2:c.1430T>A	NP_001304986.2:p.Val477Asp
NM_001331035.2:c.1385T>A	NP_001317964.1:p.Val462Asp
NM_001375278.1:c.1430T>A	NP_001362207.1:p.Val477Asp
NM_001375279.1:c.1406T>A	NP_001362208.1:p.Val469Asp
NM_001375280.1:c.1385T>A	NP_001362209.1:p.Val462Asp
NM_001375281.1:c.1406T>A	NP_001362210.1:p.Val469Asp
NM_001375282.1:c.1385T>A	NP_001362211.1:p.Val462Asp
NM_001375283.1:c.1349T>A	NP_001362212.1:p.Val450Asp
NM_001375284.1:c.797T>A	NP_001362213.1:p.Val266Asp
NR_164671.1:n.1176+2973T>A
NR_164672.1:n.1456T>A
NR_164673.1:n.1430T>A
NM_000204.5:c.1406T>A MANE Select	NP_000195.3:p.Val469Asp