Canonical Allele Identifier: CA1217769226

Gene: CFH

Linked Data

• dbSNP Id: rs1652911751

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743989_196743990del , CM000663.2:g.196743989_196743990del	GRCh38
NC_000001.10:g.196713119_196713120del , CM000663.1:g.196713119_196713120del	GRCh37
NC_000001.9:g.194979742_194979743del	NCBI36
NG_007259.1:g.96979_96980del , LRG_47:g.96979_96980del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4338+361_4338+362del
ENST00000695970.1:c.3136+361_3136+362del	ENSP00000512297.1:n.3136+361_3136+362del
ENST00000695971.1:c.3289+361_3289+362del	ENSP00000512298.1:n.3289+361_3289+362del
ENST00000695972.1:c.*387+361_*387+362del	ENSP00000512299.1:n.*387+361_*387+362del
ENST00000695973.1:c.*1674+361_*1674+362del	ENSP00000512300.1:n.*1674+361_*1674+362del
ENST00000695974.1:c.3133+361_3133+362del	ENSP00000512301.1:n.3133+361_3133+362del
ENST00000695975.1:c.*1437+361_*1437+362del	ENSP00000512302.1:n.*1437+361_*1437+362del
ENST00000695976.1:c.3121+361_3121+362del	ENSP00000512303.1:n.3121+361_3121+362del
ENST00000695981.1:c.3310+361_3310+362del	ENSP00000512306.1:n.3310+361_3310+362del
ENST00000695984.1:c.1318+361_1318+362del	ENSP00000512309.1:n.1318+361_1318+362del
ENST00000695986.1:c.*2961+361_*2961+362del	ENSP00000512311.1:n.*2961+361_*2961+362del
ENST00000696026.1:c.*1592+361_*1592+362del	ENSP00000512335.1:n.*1592+361_*1592+362del
ENST00000696027.1:c.3304+361_3304+362del	ENSP00000512336.1:n.3304+361_3304+362del
ENST00000696028.1:c.3238+361_3238+362del	ENSP00000512337.1:n.3238+361_3238+362del
ENST00000696029.1:c.3304+361_3304+362del	ENSP00000512338.1:n.3304+361_3304+362del
ENST00000696031.1:c.*2828+361_*2828+362del	ENSP00000512340.1:n.*2828+361_*2828+362del
ENST00000696032.1:c.3310+361_3310+362del	ENSP00000512341.1:n.3310+361_3310+362del
ENST00000696033.1:c.1160-35808_1160-35807del	ENSP00000512342.1:n.1160-35808_1160-35807del
ENST00000367429.9:c.3310+361_3310+362del MANE Select	ENSP00000356399.4:n.3310+361_3310+362del
ENST00000367429.8:c.3310+361_3310+362del	ENSP00000356399.4:n.3310+361_3310+362del
ENST00000466229.5:n.6408+361_6408+362del
NM_000186.3:c.3310+361_3310+362del , LRG_47t1:c.3310+361_3310+362del	NP_000177.2:n.3310+361_3310+362del
XR_001737134.2:n.3496+361_3496+362del
NM_000186.4:c.3310+361_3310+362del MANE Select	NP_000177.2:n.3310+361_3310+362del