Canonical Allele Identifier: CA2320566078

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710004_6710026delinsAGGGAGAGAGAGGGAGAGAGGGC , CM000681.2:g.6710004_6710026delinsAGGGAGAGAGAGGGAGAGAGGGC	GRCh38
NC_000019.9:g.6710015_6710037delinsAGGGAGAGAGAGGGAGAGAGGGC , CM000681.1:g.6710015_6710037delinsAGGGAGAGAGAGGGAGAGAGGGC	GRCh37
NC_000019.8:g.6661015_6661037delinsAGGGAGAGAGAGGGAGAGAGGGC	NCBI36
NG_009557.1:g.15626_15648delinsGCCCTCTCTCCCTCTCTCTCCCT , LRG_27:g.15626_15648delinsGCCCTCTCTCCCTCTCTCTCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-184_1564-162delinsGCCCTCTCTCCCTCTCTCTCCCT	ENSP00000512083.1:n.1564-184_1564-162delinsGCCCTCTCTCCCTCTCTC...
ENST00000695654.1:c.811-184_811-162delinsGCCCTCTCTCCCTCTCTCTCCCT	ENSP00000512085.1:n.811-184_811-162delinsGCCCTCTCTCCCTCTCTCTC...
ENST00000695655.1:c.592-148_592-126delinsGCCCTCTCTCCCTCTCTCTCCCT	ENSP00000512086.1:n.592-148_592-126delinsGCCCTCTCTCCCTCTCTCTC...
ENST00000695692.1:n.1051-184_1051-162delinsGCCCTCTCTCCCTCTCTCTCCCT
ENST00000245907.11:c.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTCTCCCT MANE Select	ENSP00000245907.4:n.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTC...
ENST00000245907.10:c.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTCTCCCT	ENSP00000245907.4:n.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTC...
ENST00000600763.1:n.320-184_320-162delinsGCCCTCTCTCCCTCTCTCTCCCT
NM_000064.3:c.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTCTCCCT	NP_000055.2:n.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTCTCCCT
NM_000064.4:c.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTCTCCCT MANE Select	NP_000055.2:n.1687-184_1687-162delinsGCCCTCTCTCCCTCTCTCTCCCT