Canonical Allele Identifier: CA2320566118
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710043_6710063delinsGGGAGAGACAGGGAGAGAGAC , CM000681.2:g.6710043_6710063delinsGGGAGAGACAGGGAGAGAGAC GRCh38
NC_000019.9:g.6710054_6710074delinsGGGAGAGACAGGGAGAGAGAC , CM000681.1:g.6710054_6710074delinsGGGAGAGACAGGGAGAGAGAC GRCh37
NC_000019.8:g.6661054_6661074delinsGGGAGAGACAGGGAGAGAGAC NCBI36
NG_009557.1:g.15589_15609delinsGTCTCTCTCCCTGTCTCTCCC , LRG_27:g.15589_15609delinsGTCTCTCTCCCTGTCTCTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1564-221_1564-201delinsGTCTCTCTCCCTGTCTCTCCC ENSP00000512083.1:n.1564-221_1564-201delinsGTCTCTCTCCCTGTCTCT...
ENST00000695654.1:c.811-221_811-201delinsGTCTCTCTCCCTGTCTCTCCC ENSP00000512085.1:n.811-221_811-201delinsGTCTCTCTCCCTGTCTCTCC...
ENST00000695655.1:c.592-185_592-165delinsGTCTCTCTCCCTGTCTCTCCC ENSP00000512086.1:n.592-185_592-165delinsGTCTCTCTCCCTGTCTCTCC...
ENST00000695692.1:n.1051-221_1051-201delinsGTCTCTCTCCCTGTCTCTCCC
ENST00000245907.11:c.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCTCCC MANE Select ENSP00000245907.4:n.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCT...
ENST00000245907.10:c.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCTCCC ENSP00000245907.4:n.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCT...
ENST00000600763.1:n.320-221_320-201delinsGTCTCTCTCCCTGTCTCTCCC
NM_000064.3:c.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCTCCC NP_000055.2:n.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCTCCC
NM_000064.4:c.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCTCCC MANE Select NP_000055.2:n.1687-221_1687-201delinsGTCTCTCTCCCTGTCTCTCCC