Canonical Allele Identifier: CA993073598

Gene: C3

Linked Data

• gnomAD v3: 19-6710022-AGGGCGG-A
• gnomAD v4: 19-6710022-AGGGCGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710024_6710029del , CM000681.2:g.6710024_6710029del	GRCh38
NC_000019.9:g.6710035_6710040del , CM000681.1:g.6710035_6710040del	GRCh37
NC_000019.8:g.6661035_6661040del	NCBI36
NG_009557.1:g.15624_15629del , LRG_27:g.15624_15629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-186_1564-181del	ENSP00000512083.1:n.1564-186_1564-181del
ENST00000695654.1:c.811-186_811-181del	ENSP00000512085.1:n.811-186_811-181del
ENST00000695655.1:c.592-150_592-145del	ENSP00000512086.1:n.592-150_592-145del
ENST00000695692.1:n.1051-186_1051-181del
ENST00000245907.11:c.1687-186_1687-181del MANE Select	ENSP00000245907.4:n.1687-186_1687-181del
ENST00000245907.10:c.1687-186_1687-181del	ENSP00000245907.4:n.1687-186_1687-181del
ENST00000600763.1:n.320-186_320-181del
NM_000064.3:c.1687-186_1687-181del	NP_000055.2:n.1687-186_1687-181del
NM_000064.4:c.1687-186_1687-181del MANE Select	NP_000055.2:n.1687-186_1687-181del