Canonical Allele Identifier: CA2582310855

Gene: C3

Linked Data

• gnomAD v3: 19-6710030-A-AGAGAGAGGGAGAGAGGGCGG
• gnomAD v4: 19-6710030-A-AGAGAGAGGGAGAGAGGGCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710037_6710038insGGAGAGAGGGCGGGAGAGAG , CM000681.2:g.6710037_6710038insGGAGAGAGGGCGGGAGAGAG	GRCh38
NC_000019.9:g.6710048_6710049insGGAGAGAGGGCGGGAGAGAG , CM000681.1:g.6710048_6710049insGGAGAGAGGGCGGGAGAGAG	GRCh37
NC_000019.8:g.6661048_6661049insGGAGAGAGGGCGGGAGAGAG	NCBI36
NG_009557.1:g.15621_15622insCCGCCCTCTCTCCCTCTCTC , LRG_27:g.15621_15622insCCGCCCTCTCTCCCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-189_1564-188insCCGCCCTCTCTCCCTCTCTC	ENSP00000512083.1:n.1564-189_1564-188insCCGCCCTCTCTCCCTCTCTC
ENST00000695654.1:c.811-189_811-188insCCGCCCTCTCTCCCTCTCTC	ENSP00000512085.1:n.811-189_811-188insCCGCCCTCTCTCCCTCTCTC
ENST00000695655.1:c.592-153_592-152insCCGCCCTCTCTCCCTCTCTC	ENSP00000512086.1:n.592-153_592-152insCCGCCCTCTCTCCCTCTCTC
ENST00000695692.1:n.1051-189_1051-188insCCGCCCTCTCTCCCTCTCTC
ENST00000245907.11:c.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC MANE Select	ENSP00000245907.4:n.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC
ENST00000245907.10:c.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC	ENSP00000245907.4:n.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC
ENST00000600763.1:n.320-189_320-188insCCGCCCTCTCTCCCTCTCTC
NM_000064.3:c.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC	NP_000055.2:n.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC
NM_000064.4:c.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC MANE Select	NP_000055.2:n.1687-189_1687-188insCCGCCCTCTCTCCCTCTCTC