Canonical Allele Identifier: CA2320566095

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710022_6710026delinsAGGGC , CM000681.2:g.6710022_6710026delinsAGGGC	GRCh38
NC_000019.9:g.6710033_6710037delinsAGGGC , CM000681.1:g.6710033_6710037delinsAGGGC	GRCh37
NC_000019.8:g.6661033_6661037delinsAGGGC	NCBI36
NG_009557.1:g.15626_15630delinsGCCCT , LRG_27:g.15626_15630delinsGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-184_1564-180delinsGCCCT	ENSP00000512083.1:n.1564-184_1564-180delinsGCCCT
ENST00000695654.1:c.811-184_811-180delinsGCCCT	ENSP00000512085.1:n.811-184_811-180delinsGCCCT
ENST00000695655.1:c.592-148_592-144delinsGCCCT	ENSP00000512086.1:n.592-148_592-144delinsGCCCT
ENST00000695692.1:n.1051-184_1051-180delinsGCCCT
ENST00000245907.11:c.1687-184_1687-180delinsGCCCT MANE Select	ENSP00000245907.4:n.1687-184_1687-180delinsGCCCT
ENST00000245907.10:c.1687-184_1687-180delinsGCCCT	ENSP00000245907.4:n.1687-184_1687-180delinsGCCCT
ENST00000600763.1:n.320-184_320-180delinsGCCCT
NM_000064.3:c.1687-184_1687-180delinsGCCCT	NP_000055.2:n.1687-184_1687-180delinsGCCCT
NM_000064.4:c.1687-184_1687-180delinsGCCCT MANE Select	NP_000055.2:n.1687-184_1687-180delinsGCCCT