Canonical Allele Identifier: CA2587877632

Gene: C3

Linked Data

• gnomAD v4: 19-6709980-A-AACGCAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709980_6709981insACGCAGG , CM000681.2:g.6709980_6709981insACGCAGG	GRCh38
NC_000019.9:g.6709991_6709992insACGCAGG , CM000681.1:g.6709991_6709992insACGCAGG	GRCh37
NC_000019.8:g.6660991_6660992insACGCAGG	NCBI36
NG_009557.1:g.15671_15672insCCTGCGT , LRG_27:g.15671_15672insCCTGCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-139_1564-138insCCTGCGT	ENSP00000512083.1:n.1564-139_1564-138insCCTGCGT
ENST00000695654.1:c.811-139_811-138insCCTGCGT	ENSP00000512085.1:n.811-139_811-138insCCTGCGT
ENST00000695655.1:c.592-103_592-102insCCTGCGT	ENSP00000512086.1:n.592-103_592-102insCCTGCGT
ENST00000695692.1:n.1051-139_1051-138insCCTGCGT
ENST00000245907.11:c.1687-139_1687-138insCCTGCGT MANE Select	ENSP00000245907.4:n.1687-139_1687-138insCCTGCGT
ENST00000245907.10:c.1687-139_1687-138insCCTGCGT	ENSP00000245907.4:n.1687-139_1687-138insCCTGCGT
ENST00000600763.1:n.320-139_320-138insCCTGCGT
NM_000064.3:c.1687-139_1687-138insCCTGCGT	NP_000055.2:n.1687-139_1687-138insCCTGCGT
NM_000064.4:c.1687-139_1687-138insCCTGCGT MANE Select	NP_000055.2:n.1687-139_1687-138insCCTGCGT