Canonical Allele Identifier: CA1484702718

Gene: CFI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109737838C= , CM000666.2:g.109737838C=	GRCh38
NC_000004.11:g.110658994C= , CM000666.1:g.110658994C=	GRCh37
NC_000004.10:g.110878443C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695844.1:n.1714-3042G=
ENST00000695845.1:n.1712+4653G=
ENST00000645635.1:c.1534+4653G=	ENSP00000493607.1:n.1534+4653G=
XM_011531920.1:c.1558+4653G=	XP_011530222.1:n.1558+4653G=
XM_011531920.2:c.1558+4653G=	XP_011530222.1:n.1558+4653G=
XM_017008164.2:c.1534+4653G=	XP_016863653.1:n.1534+4653G=
XM_017008165.2:c.1513+4653G=	XP_016863654.1:n.1513+4653G=
XM_017008166.2:c.1535-3038G=	XP_016863655.1:n.1535-3038G=
NM_001375278.1:c.1559-3042G=	NP_001362207.1:n.1559-3042G=
NM_001375279.1:c.1535-3042G=	NP_001362208.1:n.1535-3042G=
NM_001375280.1:c.1514-3042G=	NP_001362209.1:n.1514-3042G=
NM_001375281.1:c.1534+4653G=	NP_001362210.1:n.1534+4653G=
NM_001375282.1:c.1513+4653G=	NP_001362211.1:n.1513+4653G=