Canonical Allele Identifier: CA357853957

Gene: CFI

Linked Data

• gnomAD v4: 4-109740805-C-G
• MyVariant Identifiers: chr4:g.110661961C>G (hg19) ; chr4:g.109740805C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740805C>G , CM000666.2:g.109740805C>G	GRCh38
NC_000004.11:g.110661961C>G , CM000666.1:g.110661961C>G	GRCh37
NC_000004.10:g.110881410C>G	NCBI36
NG_007569.1:g.66181G>C , LRG_48:g.66181G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1686G>C
ENST00000695845.1:n.1712+1686G>C
ENST00000695846.1:n.1864G>C
ENST00000394634.7:c.*88G>C MANE Select	ENSP00000378130.2:n.*88G>C
ENST00000394635.8:c.*88G>C	ENSP00000378131.3:n.*88G>C
ENST00000645635.1:c.1534+1686G>C	ENSP00000493607.1:n.1534+1686G>C
ENST00000394634.6:c.*88G>C	ENSP00000378130.2:n.*88G>C
ENST00000394635.7:c.*88G>C	ENSP00000378131.3:n.*88G>C
ENST00000504853.3:n.2257G>C
ENST00000512148.5:c.*88G>C	ENSP00000427438.1:n.*88G>C
ENST00000618244.4:c.1045G>C	ENSP00000483416.1:p.Gly349Arg
NM_000204.3:c.*88G>C , LRG_48t1:c.*88G>C	NP_000195.2:n.*88G>C
XM_005262975.1:c.*88G>C	XP_005263032.1:n.*88G>C
XM_005262976.1:c.*88G>C	XP_005263033.1:n.*88G>C
XM_006714209.1:c.*88G>C	XP_006714272.1:n.*88G>C
XM_011531920.1:c.1558+1686G>C	XP_011530222.1:n.1558+1686G>C
NM_000204.4:c.*88G>C	NP_000195.2:n.*88G>C
NM_001318057.1:c.*88G>C	NP_001304986.1:n.*88G>C
NM_001331035.1:c.*88G>C	NP_001317964.1:n.*88G>C
XM_011531920.2:c.1558+1686G>C	XP_011530222.1:n.1558+1686G>C
XM_017008164.2:c.1534+1686G>C	XP_016863653.1:n.1534+1686G>C
XM_017008165.2:c.1513+1686G>C	XP_016863654.1:n.1513+1686G>C
XM_017008166.2:c.1534+1686G>C	XP_016863655.1:n.1534+1686G>C
NM_001318057.2:c.*88G>C	NP_001304986.2:n.*88G>C
NM_001331035.2:c.*88G>C	NP_001317964.1:n.*88G>C
NM_001375278.1:c.1558+1686G>C	NP_001362207.1:n.1558+1686G>C
NM_001375279.1:c.1534+1686G>C	NP_001362208.1:n.1534+1686G>C
NM_001375280.1:c.1513+1686G>C	NP_001362209.1:n.1513+1686G>C
NM_001375281.1:c.1534+1686G>C	NP_001362210.1:n.1534+1686G>C
NM_001375282.1:c.1513+1686G>C	NP_001362211.1:n.1513+1686G>C
NM_001375283.1:c.*88G>C	NP_001362212.1:n.*88G>C
NM_001375284.1:c.*88G>C	NP_001362213.1:n.*88G>C
NR_164671.1:n.1587G>C
NR_164672.1:n.1890G>C
NR_164673.1:n.1864G>C
NM_000204.5:c.*88G>C MANE Select	NP_000195.3:n.*88G>C