Canonical Allele Identifier: CA993073419

Gene: C3

Linked Data

• gnomAD v3: 19-6709991-A-AAGGGACAGAGGGAGGGAGAGAG
• gnomAD v4: 19-6709991-A-AAGGGACAGAGGGAGGGAGAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709996_6709997insCAGAGGGAGGGAGAGAGAGGGA , CM000681.2:g.6709996_6709997insCAGAGGGAGGGAGAGAGAGGGA	GRCh38
NC_000019.9:g.6710007_6710008insCAGAGGGAGGGAGAGAGAGGGA , CM000681.1:g.6710007_6710008insCAGAGGGAGGGAGAGAGAGGGA	GRCh37
NC_000019.8:g.6661007_6661008insCAGAGGGAGGGAGAGAGAGGGA	NCBI36
NG_009557.1:g.15660_15661insCTCTCTCCCTCCCTCTGTCCCT , LRG_27:g.15660_15661insCTCTCTCCCTCCCTCTGTCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-150_1564-149insCTCTCTCCCTCCCTCTGTCCCT	ENSP00000512083.1:n.1564-150_1564-149insCTCTCTCCCTCCCTCTGTCCC...
ENST00000695654.1:c.811-150_811-149insCTCTCTCCCTCCCTCTGTCCCT	ENSP00000512085.1:n.811-150_811-149insCTCTCTCCCTCCCTCTGTCCCT
ENST00000695655.1:c.592-114_592-113insCTCTCTCCCTCCCTCTGTCCCT	ENSP00000512086.1:n.592-114_592-113insCTCTCTCCCTCCCTCTGTCCCT
ENST00000695692.1:n.1051-150_1051-149insCTCTCTCCCTCCCTCTGTCCCT
ENST00000245907.11:c.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCCT MANE Select	ENSP00000245907.4:n.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCC...
ENST00000245907.10:c.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCCT	ENSP00000245907.4:n.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCC...
ENST00000600763.1:n.320-150_320-149insCTCTCTCCCTCCCTCTGTCCCT
NM_000064.3:c.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCCT	NP_000055.2:n.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCCT
NM_000064.4:c.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCCT MANE Select	NP_000055.2:n.1687-150_1687-149insCTCTCTCCCTCCCTCTGTCCCT