Canonical Allele Identifier: CA343983941

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712718G>A (hg19) ; chr1:g.196743588G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743588G>A , CM000663.2:g.196743588G>A	GRCh38
NC_000001.10:g.196712718G>A , CM000663.1:g.196712718G>A	GRCh37
NC_000001.9:g.194979341G>A	NCBI36
NG_007259.1:g.96578G>A , LRG_47:g.96578G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4298G>A
ENST00000695970.1:c.3096G>A	ENSP00000512297.1:p.Met1032Ile
ENST00000695971.1:c.3249G>A	ENSP00000512298.1:p.Met1083Ile
ENST00000695972.1:c.*347G>A	ENSP00000512299.1:n.*347G>A
ENST00000695973.1:c.*1634G>A	ENSP00000512300.1:n.*1634G>A
ENST00000695974.1:c.3093G>A	ENSP00000512301.1:p.Met1031Ile
ENST00000695975.1:c.*1397G>A	ENSP00000512302.1:n.*1397G>A
ENST00000695976.1:c.3081G>A	ENSP00000512303.1:p.Met1027Ile
ENST00000695981.1:c.3270G>A	ENSP00000512306.1:p.Met1090Ile
ENST00000695984.1:c.1278G>A	ENSP00000512309.1:p.Met426Ile
ENST00000695986.1:c.*2921G>A	ENSP00000512311.1:n.*2921G>A
ENST00000696026.1:c.*1552G>A	ENSP00000512335.1:n.*1552G>A
ENST00000696027.1:c.3264G>A	ENSP00000512336.1:p.Met1088Ile
ENST00000696028.1:c.3198G>A	ENSP00000512337.1:p.Met1066Ile
ENST00000696029.1:c.3264G>A	ENSP00000512338.1:p.Met1088Ile
ENST00000696031.1:c.*2788G>A	ENSP00000512340.1:n.*2788G>A
ENST00000696032.1:c.3270G>A	ENSP00000512341.1:p.Met1090Ile
ENST00000696033.1:c.1160-36209G>A	ENSP00000512342.1:n.1160-36209G>A
ENST00000367429.9:c.3270G>A MANE Select	ENSP00000356399.4:p.Met1090Ile
ENST00000367429.8:c.3270G>A	ENSP00000356399.4:p.Met1090Ile
ENST00000466229.5:n.6368G>A
NM_000186.3:c.3270G>A , LRG_47t1:c.3270G>A	NP_000177.2:p.Met1090Ile
XR_001737134.2:n.3456G>A
NM_000186.4:c.3270G>A MANE Select	NP_000177.2:p.Met1090Ile