Canonical Allele Identifier: CA2320567708

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712931_6712971delinsTGGACACAGACTTCATACTGGGCCTGTGCCCCCATCAGCCC , CM000681.2:g.6712931_6712971delinsTGGACACAGACTTCATACTGGGCCTGTGCCCCCATCAGCCC	GRCh38
NC_000019.9:g.6712942_6712982delinsTGGACACAGACTTCATACTGGGCCTGTGCCCCCATCAGCCC , CM000681.1:g.6712942_6712982delinsTGGACACAGACTTCATACTGGGCCTGTGCCCCCATCAGCCC	GRCh37
NC_000019.8:g.6663942_6663982delinsTGGACACAGACTTCATACTGGGCCTGTGCCCCCATCAGCCC	NCBI36
NG_009557.1:g.12681_12721delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA , LRG_27:g.12681_12721delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+218_880+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA	ENSP00000512083.1:n.880+218_880+258delinsGGGCTGATGGGGGCACAGGC...
ENST00000695654.1:c.127+218_127+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA	ENSP00000512085.1:n.127+218_127+258delinsGGGCTGATGGGGGCACAGGC...
ENST00000695692.1:n.327+218_327+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA
ENST00000245907.11:c.1003+218_1003+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA MANE Select	ENSP00000245907.4:n.1003+218_1003+258delinsGGGCTGATGGGGGCACAG...
ENST00000245907.10:c.1003+218_1003+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA	ENSP00000245907.4:n.1003+218_1003+258delinsGGGCTGATGGGGGCACAG...
ENST00000594270.5:n.127+218_127+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA
ENST00000595577.1:n.507+218_507+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA
ENST00000597442.5:n.253+218_253+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA
NM_000064.3:c.1003+218_1003+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA	NP_000055.2:n.1003+218_1003+258delinsGGGCTGATGGGGGCACAGGCCCAG...
NM_000064.4:c.1003+218_1003+258delinsGGGCTGATGGGGGCACAGGCCCAGTATGAAGTCTGTGTCCA MANE Select	NP_000055.2:n.1003+218_1003+258delinsGGGCTGATGGGGGCACAGGCCCAG...