Canonical Allele Identifier: CA357854727

Gene: CFI

Linked Data

• MyVariant Identifiers: chr4:g.110662258C>G (hg19) ; chr4:g.109741102C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109741102C>G , CM000666.2:g.109741102C>G	GRCh38
NC_000004.11:g.110662258C>G , CM000666.1:g.110662258C>G	GRCh37
NC_000004.10:g.110881707C>G	NCBI36
NG_007569.1:g.65884G>C , LRG_48:g.65884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1389G>C
ENST00000695845.1:n.1712+1389G>C
ENST00000695846.1:n.1567G>C
ENST00000394634.7:c.1543G>C MANE Select	ENSP00000378130.2:p.Asp515His
ENST00000394635.8:c.1567G>C	ENSP00000378131.3:p.Asp523His
ENST00000645635.1:c.1534+1389G>C	ENSP00000493607.1:n.1534+1389G>C
ENST00000394634.6:c.1543G>C	ENSP00000378130.2:p.Asp515His
ENST00000394635.7:c.1567G>C	ENSP00000378131.3:p.Asp523His
ENST00000504853.3:n.1960G>C
ENST00000512148.5:c.1522G>C	ENSP00000427438.1:p.Asp508His
ENST00000618244.4:c.1045-297G>C	ENSP00000483416.1:n.1045-297G>C
NM_000204.3:c.1543G>C , LRG_48t1:c.1543G>C	NP_000195.2:p.Asp515His
XM_005262975.1:c.1567G>C	XP_005263032.1:p.Asp523His
XM_005262976.1:c.1522G>C	XP_005263033.1:p.Asp508His
XM_006714209.1:c.1564G>C	XP_006714272.1:p.Asp522His
XM_011531920.1:c.1558+1389G>C	XP_011530222.1:n.1558+1389G>C
NM_000204.4:c.1543G>C	NP_000195.2:p.Asp515His
NM_001318057.1:c.1567G>C	NP_001304986.1:p.Asp523His
NM_001331035.1:c.1522G>C	NP_001317964.1:p.Asp508His
XM_011531920.2:c.1558+1389G>C	XP_011530222.1:n.1558+1389G>C
XM_017008164.2:c.1534+1389G>C	XP_016863653.1:n.1534+1389G>C
XM_017008165.2:c.1513+1389G>C	XP_016863654.1:n.1513+1389G>C
XM_017008166.2:c.1534+1389G>C	XP_016863655.1:n.1534+1389G>C
NM_001318057.2:c.1567G>C	NP_001304986.2:p.Asp523His
NM_001331035.2:c.1522G>C	NP_001317964.1:p.Asp508His
NM_001375278.1:c.1558+1389G>C	NP_001362207.1:n.1558+1389G>C
NM_001375279.1:c.1534+1389G>C	NP_001362208.1:n.1534+1389G>C
NM_001375280.1:c.1513+1389G>C	NP_001362209.1:n.1513+1389G>C
NM_001375281.1:c.1534+1389G>C	NP_001362210.1:n.1534+1389G>C
NM_001375282.1:c.1513+1389G>C	NP_001362211.1:n.1513+1389G>C
NM_001375283.1:c.1486G>C	NP_001362212.1:p.Asp496His
NM_001375284.1:c.934G>C	NP_001362213.1:p.Asp312His
NR_164671.1:n.1290G>C
NR_164672.1:n.1593G>C
NR_164673.1:n.1567G>C
NM_000204.5:c.1543G>C MANE Select	NP_000195.3:p.Asp515His