Canonical Allele Identifier: CA2587877660

Gene: C3

Linked Data

• gnomAD v4: 19-6709991-A-AAGGGAGAGAGGGAGGGGGAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710007_6710008insGGAGAGAGGGAGAGAGGGAGGG , CM000681.2:g.6710007_6710008insGGAGAGAGGGAGAGAGGGAGGG	GRCh38
NC_000019.9:g.6710018_6710019insGGAGAGAGGGAGAGAGGGAGGG , CM000681.1:g.6710018_6710019insGGAGAGAGGGAGAGAGGGAGGG	GRCh37
NC_000019.8:g.6661018_6661019insGGAGAGAGGGAGAGAGGGAGGG	NCBI36
NG_009557.1:g.15660_15661insCTCTCCCCCTCCCTCTCTCCCT , LRG_27:g.15660_15661insCTCTCCCCCTCCCTCTCTCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-150_1564-149insCTCTCCCCCTCCCTCTCTCCCT	ENSP00000512083.1:n.1564-150_1564-149insCTCTCCCCCTCCCTCTCTCCC...
ENST00000695654.1:c.811-150_811-149insCTCTCCCCCTCCCTCTCTCCCT	ENSP00000512085.1:n.811-150_811-149insCTCTCCCCCTCCCTCTCTCCCT
ENST00000695655.1:c.592-114_592-113insCTCTCCCCCTCCCTCTCTCCCT	ENSP00000512086.1:n.592-114_592-113insCTCTCCCCCTCCCTCTCTCCCT
ENST00000695692.1:n.1051-150_1051-149insCTCTCCCCCTCCCTCTCTCCCT
ENST00000245907.11:c.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCCT MANE Select	ENSP00000245907.4:n.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCC...
ENST00000245907.10:c.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCCT	ENSP00000245907.4:n.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCC...
ENST00000600763.1:n.320-150_320-149insCTCTCCCCCTCCCTCTCTCCCT
NM_000064.3:c.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCCT	NP_000055.2:n.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCCT
NM_000064.4:c.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCCT MANE Select	NP_000055.2:n.1687-150_1687-149insCTCTCCCCCTCCCTCTCTCCCT