Canonical Allele Identifier: CA103685788

Gene: CFI

Linked Data

• dbSNP Id: rs35201237
• MyVariant Identifiers: chr4:g.110658974_110658975insC (hg19) ; chr4:g.109737818_109737819insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109737818_109737819insC , CM000666.2:g.109737818_109737819insC	GRCh38
NC_000004.11:g.110658974_110658975insC , CM000666.1:g.110658974_110658975insC	GRCh37
NC_000004.10:g.110878423_110878424insC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000695844.1:n.1714-3023_1714-3022insG
ENST00000695845.1:n.1712+4672_1712+4673insG
ENST00000645635.1:c.1534+4672_1534+4673insG	ENSP00000493607.1:n.1534+4672_1534+4673in...
XM_011531920.1:c.1558+4672_1558+4673insG	XP_011530222.1:n.1558+4672_1558+4673insG
XM_011531920.2:c.1558+4672_1558+4673insG	XP_011530222.1:n.1558+4672_1558+4673insG
XM_017008164.2:c.1534+4672_1534+4673insG	XP_016863653.1:n.1534+4672_1534+4673insG
XM_017008165.2:c.1513+4672_1513+4673insG	XP_016863654.1:n.1513+4672_1513+4673insG
XM_017008166.2:c.1535-3019_1535-3018insG	XP_016863655.1:n.1535-3019_1535-3018insG
NM_001375278.1:c.1559-3023_1559-3022insG	NP_001362207.1:n.1559-3023_1559-3022insG
NM_001375279.1:c.1535-3023_1535-3022insG	NP_001362208.1:n.1535-3023_1535-3022insG
NM_001375280.1:c.1514-3023_1514-3022insG	NP_001362209.1:n.1514-3023_1514-3022insG
NM_001375281.1:c.1534+4672_1534+4673insG	NP_001362210.1:n.1534+4672_1534+4673insG
NM_001375282.1:c.1513+4672_1513+4673insG	NP_001362211.1:n.1513+4672_1513+4673insG