Canonical Allele Identifier: CA1484702731

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109737875G= , CM000666.2:g.109737875G=	GRCh38
NC_000004.11:g.110659031G= , CM000666.1:g.110659031G=	GRCh37
NC_000004.10:g.110878480G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000695844.1:n.1714-3079C=
ENST00000695845.1:n.1712+4616C=
ENST00000645635.1:c.1534+4616C=	ENSP00000493607.1:n.1534+4616C=
XM_011531920.1:c.1558+4616C=	XP_011530222.1:n.1558+4616C=
XM_011531920.2:c.1558+4616C=	XP_011530222.1:n.1558+4616C=
XM_017008164.2:c.1534+4616C=	XP_016863653.1:n.1534+4616C=
XM_017008165.2:c.1513+4616C=	XP_016863654.1:n.1513+4616C=
XM_017008166.2:c.1535-3075C=	XP_016863655.1:n.1535-3075C=
NM_001375278.1:c.1559-3079C=	NP_001362207.1:n.1559-3079C=
NM_001375279.1:c.1535-3079C=	NP_001362208.1:n.1535-3079C=
NM_001375280.1:c.1514-3079C=	NP_001362209.1:n.1514-3079C=
NM_001375281.1:c.1534+4616C=	NP_001362210.1:n.1534+4616C=
NM_001375282.1:c.1513+4616C=	NP_001362211.1:n.1513+4616C=