Canonical Allele Identifier: CA2697554820

Gene: CFH

Linked Data

• ClinVar Variation Id: 2745673
• ClinVar RCV Id: RCV003568156

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196740795dup , CM000663.2:g.196740795dup	GRCh38
NC_000001.10:g.196709925dup , CM000663.1:g.196709925dup	GRCh37
NC_000001.9:g.194976548dup	NCBI36
NG_007259.1:g.93785dup , LRG_47:g.93785dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.3225dup
ENST00000695970.1:c.2783-1080dup	ENSP00000512297.1:n.2783-1080dup
ENST00000695971.1:c.2935+3dup	ENSP00000512298.1:n.2935+3dup
ENST00000695972.1:c.*33+3dup	ENSP00000512299.1:n.*33+3dup
ENST00000695973.1:c.*1320+3dup	ENSP00000512300.1:n.*1320+3dup
ENST00000695974.1:c.2779+3dup	ENSP00000512301.1:n.2779+3dup
ENST00000695975.1:c.*1083+3dup	ENSP00000512302.1:n.*1083+3dup
ENST00000695976.1:c.2767+3dup	ENSP00000512303.1:n.2767+3dup
ENST00000695981.1:c.2956+3dup	ENSP00000512306.1:n.2956+3dup
ENST00000695983.1:c.2862+97dup	ENSP00000512308.1:n.2862+97dup
ENST00000695984.1:c.964+3dup	ENSP00000512309.1:n.964+3dup
ENST00000695986.1:c.*2607+3dup	ENSP00000512311.1:n.*2607+3dup
ENST00000696025.1:n.3043dup
ENST00000696026.1:c.*1238+3dup	ENSP00000512335.1:n.*1238+3dup
ENST00000696027.1:c.2950+3dup	ENSP00000512336.1:n.2950+3dup
ENST00000696028.1:c.2884+75dup	ENSP00000512337.1:n.2884+75dup
ENST00000696029.1:c.2956+3dup	ENSP00000512338.1:n.2956+3dup
ENST00000696031.1:c.*2474+3dup	ENSP00000512340.1:n.*2474+3dup
ENST00000696032.1:c.2956+3dup	ENSP00000512341.1:n.2956+3dup
ENST00000696033.1:c.1160-39002dup	ENSP00000512342.1:n.1160-39002dup
ENST00000367429.9:c.2956+3dup MANE Select	ENSP00000356399.4:n.2956+3dup
ENST00000367429.8:c.2956+3dup	ENSP00000356399.4:n.2956+3dup
ENST00000466229.5:n.4975dup
ENST00000470918.1:n.462dup
NM_000186.3:c.2956+3dup , LRG_47t1:c.2956+3dup	NP_000177.2:n.2956+3dup
XR_001737134.2:n.3142+3dup
NM_000186.4:c.2956+3dup MANE Select	NP_000177.2:n.2956+3dup