Canonical Allele Identifier: CA2813446553

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710005_6710006insCGAGAGAGAGGGAGAGAGGGAG , CM000681.2:g.6710005_6710006insCGAGAGAGAGGGAGAGAGGGAG	GRCh38
NC_000019.9:g.6710016_6710017insCGAGAGAGAGGGAGAGAGGGAG , CM000681.1:g.6710016_6710017insCGAGAGAGAGGGAGAGAGGGAG	GRCh37
NC_000019.8:g.6661016_6661017insCGAGAGAGAGGGAGAGAGGGAG	NCBI36
NG_009557.1:g.15660_15661insCTCTCTCGCTCCCTCTCTCCCT , LRG_27:g.15660_15661insCTCTCTCGCTCCCTCTCTCCCT

Transcript Alleles

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