Canonical Allele Identifier: CA2320566115
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710041_6710071delinsAAGGGAGAGACAGGGAGAGAGACGGAGAGAC , CM000681.2:g.6710041_6710071delinsAAGGGAGAGACAGGGAGAGAGACGGAGAGAC GRCh38
NC_000019.9:g.6710052_6710082delinsAAGGGAGAGACAGGGAGAGAGACGGAGAGAC , CM000681.1:g.6710052_6710082delinsAAGGGAGAGACAGGGAGAGAGACGGAGAGAC GRCh37
NC_000019.8:g.6661052_6661082delinsAAGGGAGAGACAGGGAGAGAGACGGAGAGAC NCBI36
NG_009557.1:g.15581_15611delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT , LRG_27:g.15581_15611delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-229_1564-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT ENSP00000512083.1:n.1564-229_1564-199delinsGTCTCTCCGTCTCTCTCC...
ENST00000695654.1:c.811-229_811-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT ENSP00000512085.1:n.811-229_811-199delinsGTCTCTCCGTCTCTCTCCCT...
ENST00000695655.1:c.592-193_592-163delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT ENSP00000512086.1:n.592-193_592-163delinsGTCTCTCCGTCTCTCTCCCT...
ENST00000695692.1:n.1051-229_1051-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT
ENST00000245907.11:c.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT MANE Select ENSP00000245907.4:n.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCC...
ENST00000245907.10:c.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT ENSP00000245907.4:n.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCC...
ENST00000600763.1:n.320-229_320-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT
NM_000064.3:c.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT NP_000055.2:n.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCCCTGTCT...
NM_000064.4:c.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCCCTGTCTCTCCCTT MANE Select NP_000055.2:n.1687-229_1687-199delinsGTCTCTCCGTCTCTCTCCCTGTCT...