Canonical Allele Identifier: CA357854569

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110662188G>T (hg19) ; chr4:g.109741032G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741032G>T , CM000666.2:g.109741032G>T	GRCh38
NC_000004.11:g.110662188G>T , CM000666.1:g.110662188G>T	GRCh37
NC_000004.10:g.110881637G>T	NCBI36
NG_007569.1:g.65954C>A , LRG_48:g.65954C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1459C>A
ENST00000695845.1:n.1712+1459C>A
ENST00000695846.1:n.1637C>A
ENST00000394634.7:c.1613C>A MANE Select	ENSP00000378130.2:p.Thr538Asn
ENST00000394635.8:c.1637C>A	ENSP00000378131.3:p.Thr546Asn
ENST00000645635.1:c.1534+1459C>A	ENSP00000493607.1:n.1534+1459C>A
ENST00000394634.6:c.1613C>A	ENSP00000378130.2:p.Thr538Asn
ENST00000394635.7:c.1637C>A	ENSP00000378131.3:p.Thr546Asn
ENST00000504853.3:n.2030C>A
ENST00000512148.5:c.1592C>A	ENSP00000427438.1:p.Thr531Asn
ENST00000618244.4:c.1045-227C>A	ENSP00000483416.1:n.1045-227C>A
NM_000204.3:c.1613C>A , LRG_48t1:c.1613C>A	NP_000195.2:p.Thr538Asn
XM_005262975.1:c.1637C>A	XP_005263032.1:p.Thr546Asn
XM_005262976.1:c.1592C>A	XP_005263033.1:p.Thr531Asn
XM_006714209.1:c.1634C>A	XP_006714272.1:p.Thr545Asn
XM_011531920.1:c.1558+1459C>A	XP_011530222.1:n.1558+1459C>A
NM_000204.4:c.1613C>A	NP_000195.2:p.Thr538Asn
NM_001318057.1:c.1637C>A	NP_001304986.1:p.Thr546Asn
NM_001331035.1:c.1592C>A	NP_001317964.1:p.Thr531Asn
XM_011531920.2:c.1558+1459C>A	XP_011530222.1:n.1558+1459C>A
XM_017008164.2:c.1534+1459C>A	XP_016863653.1:n.1534+1459C>A
XM_017008165.2:c.1513+1459C>A	XP_016863654.1:n.1513+1459C>A
XM_017008166.2:c.1534+1459C>A	XP_016863655.1:n.1534+1459C>A
NM_001318057.2:c.1637C>A	NP_001304986.2:p.Thr546Asn
NM_001331035.2:c.1592C>A	NP_001317964.1:p.Thr531Asn
NM_001375278.1:c.1558+1459C>A	NP_001362207.1:n.1558+1459C>A
NM_001375279.1:c.1534+1459C>A	NP_001362208.1:n.1534+1459C>A
NM_001375280.1:c.1513+1459C>A	NP_001362209.1:n.1513+1459C>A
NM_001375281.1:c.1534+1459C>A	NP_001362210.1:n.1534+1459C>A
NM_001375282.1:c.1513+1459C>A	NP_001362211.1:n.1513+1459C>A
NM_001375283.1:c.1556C>A	NP_001362212.1:p.Thr519Asn
NM_001375284.1:c.1004C>A	NP_001362213.1:p.Thr335Asn
NR_164671.1:n.1360C>A
NR_164672.1:n.1663C>A
NR_164673.1:n.1637C>A
NM_000204.5:c.1613C>A MANE Select	NP_000195.3:p.Thr538Asn