Canonical Allele Identifier: CA2813446559

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGGGAGCGAGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGGGAGCGAGGG	GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGGGAGCGAGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGGGAGCGAGGG	GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGGGAGCGAGGG	NCBI36
NG_009557.1:g.15631_15632insGCTCCCTCTCTCTCCCTCCCTC , LRG_27:g.15631_15632insGCTCCCTCTCTCTCCCTCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-179_1564-178insGCTCCCTCTCTCTCCCTCCCTC	ENSP00000512083.1:n.1564-179_1564-178insGCTCCCTCTCTCTCCCTCCCT...
ENST00000695654.1:c.811-179_811-178insGCTCCCTCTCTCTCCCTCCCTC	ENSP00000512085.1:n.811-179_811-178insGCTCCCTCTCTCTCCCTCCCTC
ENST00000695655.1:c.592-143_592-142insGCTCCCTCTCTCTCCCTCCCTC	ENSP00000512086.1:n.592-143_592-142insGCTCCCTCTCTCTCCCTCCCTC
ENST00000695692.1:n.1051-179_1051-178insGCTCCCTCTCTCTCCCTCCCTC
ENST00000245907.11:c.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCTC MANE Select	ENSP00000245907.4:n.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCT...
ENST00000245907.10:c.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCTC	ENSP00000245907.4:n.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCT...
ENST00000600763.1:n.320-179_320-178insGCTCCCTCTCTCTCCCTCCCTC
NM_000064.3:c.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCTC	NP_000055.2:n.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCTC
NM_000064.4:c.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCTC MANE Select	NP_000055.2:n.1687-179_1687-178insGCTCCCTCTCTCTCCCTCCCTC