Canonical Allele Identifier: CA357854705

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110662248A>G (hg19) ; chr4:g.109741092A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741092A>G , CM000666.2:g.109741092A>G	GRCh38
NC_000004.11:g.110662248A>G , CM000666.1:g.110662248A>G	GRCh37
NC_000004.10:g.110881697A>G	NCBI36
NG_007569.1:g.65894T>C , LRG_48:g.65894T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1399T>C
ENST00000695845.1:n.1712+1399T>C
ENST00000695846.1:n.1577T>C
ENST00000394634.7:c.1553T>C MANE Select	ENSP00000378130.2:p.Ile518Thr
ENST00000394635.8:c.1577T>C	ENSP00000378131.3:p.Ile526Thr
ENST00000645635.1:c.1534+1399T>C	ENSP00000493607.1:n.1534+1399T>C
ENST00000394634.6:c.1553T>C	ENSP00000378130.2:p.Ile518Thr
ENST00000394635.7:c.1577T>C	ENSP00000378131.3:p.Ile526Thr
ENST00000504853.3:n.1970T>C
ENST00000512148.5:c.1532T>C	ENSP00000427438.1:p.Ile511Thr
ENST00000618244.4:c.1045-287T>C	ENSP00000483416.1:n.1045-287T>C
NM_000204.3:c.1553T>C , LRG_48t1:c.1553T>C	NP_000195.2:p.Ile518Thr
XM_005262975.1:c.1577T>C	XP_005263032.1:p.Ile526Thr
XM_005262976.1:c.1532T>C	XP_005263033.1:p.Ile511Thr
XM_006714209.1:c.1574T>C	XP_006714272.1:p.Ile525Thr
XM_011531920.1:c.1558+1399T>C	XP_011530222.1:n.1558+1399T>C
NM_000204.4:c.1553T>C	NP_000195.2:p.Ile518Thr
NM_001318057.1:c.1577T>C	NP_001304986.1:p.Ile526Thr
NM_001331035.1:c.1532T>C	NP_001317964.1:p.Ile511Thr
XM_011531920.2:c.1558+1399T>C	XP_011530222.1:n.1558+1399T>C
XM_017008164.2:c.1534+1399T>C	XP_016863653.1:n.1534+1399T>C
XM_017008165.2:c.1513+1399T>C	XP_016863654.1:n.1513+1399T>C
XM_017008166.2:c.1534+1399T>C	XP_016863655.1:n.1534+1399T>C
NM_001318057.2:c.1577T>C	NP_001304986.2:p.Ile526Thr
NM_001331035.2:c.1532T>C	NP_001317964.1:p.Ile511Thr
NM_001375278.1:c.1558+1399T>C	NP_001362207.1:n.1558+1399T>C
NM_001375279.1:c.1534+1399T>C	NP_001362208.1:n.1534+1399T>C
NM_001375280.1:c.1513+1399T>C	NP_001362209.1:n.1513+1399T>C
NM_001375281.1:c.1534+1399T>C	NP_001362210.1:n.1534+1399T>C
NM_001375282.1:c.1513+1399T>C	NP_001362211.1:n.1513+1399T>C
NM_001375283.1:c.1496T>C	NP_001362212.1:p.Ile499Thr
NM_001375284.1:c.944T>C	NP_001362213.1:p.Ile315Thr
NR_164671.1:n.1300T>C
NR_164672.1:n.1603T>C
NR_164673.1:n.1577T>C
NM_000204.5:c.1553T>C MANE Select	NP_000195.3:p.Ile518Thr