Canonical Allele Identifier: CA2671741348

Gene: CFI

Linked Data

• gnomAD v4: 4-109740604-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740604G>C , CM000666.2:g.109740604G>C	GRCh38
NC_000004.11:g.110661760G>C , CM000666.1:g.110661760G>C	GRCh37
NC_000004.10:g.110881209G>C	NCBI36
NG_007569.1:g.66382C>G , LRG_48:g.66382C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1887C>G
ENST00000695845.1:n.1712+1887C>G
ENST00000645635.1:c.1534+1887C>G	ENSP00000493607.1:n.1534+1887C>G
XM_011531920.1:c.1558+1887C>G	XP_011530222.1:n.1558+1887C>G
XM_011531920.2:c.1558+1887C>G	XP_011530222.1:n.1558+1887C>G
XM_017008164.2:c.1534+1887C>G	XP_016863653.1:n.1534+1887C>G
XM_017008165.2:c.1513+1887C>G	XP_016863654.1:n.1513+1887C>G
XM_017008166.2:c.1534+1887C>G	XP_016863655.1:n.1534+1887C>G
NM_001375278.1:c.1558+1887C>G	NP_001362207.1:n.1558+1887C>G
NM_001375279.1:c.1534+1887C>G	NP_001362208.1:n.1534+1887C>G
NM_001375280.1:c.1513+1887C>G	NP_001362209.1:n.1513+1887C>G
NM_001375281.1:c.1534+1887C>G	NP_001362210.1:n.1534+1887C>G
NM_001375282.1:c.1513+1887C>G	NP_001362211.1:n.1513+1887C>G