Canonical Allele Identifier: CA2763038089

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109740593A>G , CM000666.2:g.109740593A>G	GRCh38
NC_000004.11:g.110661749A>G , CM000666.1:g.110661749A>G	GRCh37
NC_000004.10:g.110881198A>G	NCBI36
NG_007569.1:g.66393T>C , LRG_48:g.66393T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1713+1898T>C
ENST00000695845.1:n.1712+1898T>C
ENST00000645635.1:c.1534+1898T>C	ENSP00000493607.1:n.1534+1898T>C
XM_011531920.1:c.1558+1898T>C	XP_011530222.1:n.1558+1898T>C
XM_011531920.2:c.1558+1898T>C	XP_011530222.1:n.1558+1898T>C
XM_017008164.2:c.1534+1898T>C	XP_016863653.1:n.1534+1898T>C
XM_017008165.2:c.1513+1898T>C	XP_016863654.1:n.1513+1898T>C
XM_017008166.2:c.1534+1898T>C	XP_016863655.1:n.1534+1898T>C
NM_001375278.1:c.1558+1898T>C	NP_001362207.1:n.1558+1898T>C
NM_001375279.1:c.1534+1898T>C	NP_001362208.1:n.1534+1898T>C
NM_001375280.1:c.1513+1898T>C	NP_001362209.1:n.1513+1898T>C
NM_001375281.1:c.1534+1898T>C	NP_001362210.1:n.1534+1898T>C
NM_001375282.1:c.1513+1898T>C	NP_001362211.1:n.1513+1898T>C