Canonical Allele Identifier: CA1217755606

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196714022_196714023delinsGA , CM000663.2:g.196714022_196714023delinsGA	GRCh38
NC_000001.10:g.196683152_196683153delinsGA , CM000663.1:g.196683152_196683153delinsGA	GRCh37
NC_000001.9:g.194949775_194949776delinsGA	NCBI36
NG_007259.1:g.67012_67013delinsGA , LRG_47:g.67012_67013delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.1785+105_1785+106delinsGA
ENST00000695969.1:c.1519+105_1519+106delinsGA	ENSP00000512296.1:n.1519+105_1519+106delinsGA
ENST00000695970.1:c.1519+105_1519+106delinsGA	ENSP00000512297.1:n.1519+105_1519+106delinsGA
ENST00000695971.1:c.1498+105_1498+106delinsGA	ENSP00000512298.1:n.1498+105_1498+106delinsGA
ENST00000695972.1:c.1519+105_1519+106delinsGA	ENSP00000512299.1:n.1519+105_1519+106delinsGA
ENST00000695973.1:c.1519+105_1519+106delinsGA	ENSP00000512300.1:n.1519+105_1519+106delinsGA
ENST00000695974.1:c.1519+105_1519+106delinsGA	ENSP00000512301.1:n.1519+105_1519+106delinsGA
ENST00000695975.1:c.1519+105_1519+106delinsGA	ENSP00000512302.1:n.1519+105_1519+106delinsGA
ENST00000695976.1:c.1330+105_1330+106delinsGA	ENSP00000512303.1:n.1330+105_1330+106delinsGA
ENST00000695981.1:c.1519+105_1519+106delinsGA	ENSP00000512306.1:n.1519+105_1519+106delinsGA
ENST00000695983.1:c.1519+105_1519+106delinsGA	ENSP00000512308.1:n.1519+105_1519+106delinsGA
ENST00000695984.1:c.245-14324_245-14323delinsGA	ENSP00000512309.1:n.245-14324_245-14323delinsGA
ENST00000695986.1:c.*1170+105_*1170+106delinsGA	ENSP00000512311.1:n.*1170+105_*1170+106delinsGA
ENST00000696024.1:n.1603+105_1603+106delinsGA
ENST00000696025.1:n.1603+105_1603+106delinsGA
ENST00000696026.1:c.1519+105_1519+106delinsGA	ENSP00000512335.1:n.1519+105_1519+106delinsGA
ENST00000696027.1:c.1519+105_1519+106delinsGA	ENSP00000512336.1:n.1519+105_1519+106delinsGA
ENST00000696028.1:c.1519+105_1519+106delinsGA	ENSP00000512337.1:n.1519+105_1519+106delinsGA
ENST00000696029.1:c.1519+105_1519+106delinsGA	ENSP00000512338.1:n.1519+105_1519+106delinsGA
ENST00000696031.1:c.*1037+105_*1037+106delinsGA	ENSP00000512340.1:n.*1037+105_*1037+106delinsGA
ENST00000696032.1:c.1519+105_1519+106delinsGA	ENSP00000512341.1:n.1519+105_1519+106delinsGA
ENST00000696033.1:c.1159+24408_1159+24409delinsGA	ENSP00000512342.1:n.1159+24408_1159+24409delinsGA
ENST00000367429.9:c.1519+105_1519+106delinsGA MANE Select	ENSP00000356399.4:n.1519+105_1519+106delinsGA
ENST00000367429.8:c.1519+105_1519+106delinsGA	ENSP00000356399.4:n.1519+105_1519+106delinsGA
ENST00000466229.5:n.3535+105_3535+106delinsGA
NM_000186.3:c.1519+105_1519+106delinsGA , LRG_47t1:c.1519+105_1519+106delinsGA	NP_000177.2:n.1519+105_1519+106delinsGA
XR_001737134.2:n.1604+105_1604+106delinsGA
NM_000186.4:c.1519+105_1519+106delinsGA MANE Select	NP_000177.2:n.1519+105_1519+106delinsGA