Canonical Allele Identifier: CA2735579718

Gene: C3

Linked Data

• dbSNP Id: rs2145426246

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGGGAGAGAGGGAGATAGGG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGGGAGAGAGGGAGATAGGG	GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGGGAGAGAGGGAGATAGGG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGGGAGAGAGGGAGATAGGG	GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGGGAGAGAGGGAGATAGGG	NCBI36
NG_009557.1:g.15630_15631insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT , LRG_27:g.15630_15631insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-180_1564-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT	ENSP00000512083.1:n.1564-180_1564-179insATCTCCCTCTCTCCCTCTCTC...
ENST00000695654.1:c.811-180_811-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT	ENSP00000512085.1:n.811-180_811-179insATCTCCCTCTCTCCCTCTCTCTC...
ENST00000695655.1:c.592-144_592-143insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT	ENSP00000512086.1:n.592-144_592-143insATCTCCCTCTCTCCCTCTCTCTC...
ENST00000695692.1:n.1051-180_1051-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT
ENST00000245907.11:c.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT MANE Select	ENSP00000245907.4:n.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTC...
ENST00000245907.10:c.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT	ENSP00000245907.4:n.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTC...
ENST00000600763.1:n.320-180_320-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT
NM_000064.3:c.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT	NP_000055.2:n.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTCTCCCTC...
NM_000064.4:c.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTCTCCCTCCCT MANE Select	NP_000055.2:n.1687-180_1687-179insATCTCCCTCTCTCCCTCTCTCTCCCTC...