Canonical Allele Identifier: CA2763038014

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109737828C>A , CM000666.2:g.109737828C>A	GRCh38
NC_000004.11:g.110658984C>A , CM000666.1:g.110658984C>A	GRCh37
NC_000004.10:g.110878433C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1714-3032G>T
ENST00000695845.1:n.1712+4663G>T
ENST00000645635.1:c.1534+4663G>T	ENSP00000493607.1:n.1534+4663G>T
XM_011531920.1:c.1558+4663G>T	XP_011530222.1:n.1558+4663G>T
XM_011531920.2:c.1558+4663G>T	XP_011530222.1:n.1558+4663G>T
XM_017008164.2:c.1534+4663G>T	XP_016863653.1:n.1534+4663G>T
XM_017008165.2:c.1513+4663G>T	XP_016863654.1:n.1513+4663G>T
XM_017008166.2:c.1535-3028G>T	XP_016863655.1:n.1535-3028G>T
NM_001375278.1:c.1559-3032G>T	NP_001362207.1:n.1559-3032G>T
NM_001375279.1:c.1535-3032G>T	NP_001362208.1:n.1535-3032G>T
NM_001375280.1:c.1514-3032G>T	NP_001362209.1:n.1514-3032G>T
NM_001375281.1:c.1534+4663G>T	NP_001362210.1:n.1534+4663G>T
NM_001375282.1:c.1513+4663G>T	NP_001362211.1:n.1513+4663G>T