Canonical Allele Identifier: CA2320566107

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710031_6710226delinsGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGAGAGGGAGAGAGAGAGGGAAAGAGAGAAGGAGAGAAAGAGGGAGAGAGAA , CM000681.2:g.6710031_6710226delinsGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGAGAGGGAGAGAGAGAGGGAAAGAGAGAAGGAGAGAAAGAGGGAGAGAGAA	GRCh38
NC_000019.9:g.6710042_6710237delinsGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGAGAGGGAGAGAGAGAGGGAAAGAGAGAAGGAGAGAAAGAGGGAGAGAGAA , CM000681.1:g.6710042_6710237delinsGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGAGAGGGAGAGAGAGAGGGAAAGAGAGAAGGAGAGAAAGAGGGAGAGAGAA	GRCh37
NC_000019.8:g.6661042_6661237delinsGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGAGAGGGAGAGAGAGAGGGAAAGAGAGAAGGAGAGAAAGAGGGAGAGAGAA	NCBI36
NG_009557.1:g.15426_15621delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC , LRG_27:g.15426_15621delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-384_1564-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC	ENSP00000512083.1:n.1564-384_1564-189delinsTTCTCTCTCCCTCTTTCT...
ENST00000695654.1:c.811-384_811-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC	ENSP00000512085.1:n.811-384_811-189delinsTTCTCTCTCCCTCTTTCTCT...
ENST00000695655.1:c.592-348_592-153delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC	ENSP00000512086.1:n.592-348_592-153delinsTTCTCTCTCCCTCTTTCTCT...
ENST00000695692.1:n.1051-384_1051-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC
ENST00000245907.11:c.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC MANE Select	ENSP00000245907.4:n.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCT...
ENST00000245907.10:c.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC	ENSP00000245907.4:n.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCT...
ENST00000600763.1:n.320-384_320-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC
NM_000064.3:c.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC	NP_000055.2:n.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCTCTCCTT...
NM_000064.4:c.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCTCTCCTTCTCTCTTTCCCTCTCTCTCTCCCTCTCTCTTTCCCTCTCTCTCCCTCTCCCTTTCTCTCCCTCTTTCCCTTTCCCTCTCTCCCCCCTCACTCTCCCTCTCTCTGTCTCTCCGTCTCTCTCCCTCTCTCCCTGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTTTCTCTCTCTC MANE Select	NP_000055.2:n.1687-384_1687-189delinsTTCTCTCTCCCTCTTTCTCTCCTT...