Canonical Allele Identifier: CA993073362

Gene: C3

Linked Data

• gnomAD v3: 19-6709988-A-AAG
• gnomAD v4: 19-6709988-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709988_6709989insAG , CM000681.2:g.6709988_6709989insAG	GRCh38
NC_000019.9:g.6709999_6710000insAG , CM000681.1:g.6709999_6710000insAG	GRCh37
NC_000019.8:g.6660999_6661000insAG	NCBI36
NG_009557.1:g.15663_15664insCT , LRG_27:g.15663_15664insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-147_1564-146insCT	ENSP00000512083.1:n.1564-147_1564-146insCT
ENST00000695654.1:c.811-147_811-146insCT	ENSP00000512085.1:n.811-147_811-146insCT
ENST00000695655.1:c.592-111_592-110insCT	ENSP00000512086.1:n.592-111_592-110insCT
ENST00000695692.1:n.1051-147_1051-146insCT
ENST00000245907.11:c.1687-147_1687-146insCT MANE Select	ENSP00000245907.4:n.1687-147_1687-146insCT
ENST00000245907.10:c.1687-147_1687-146insCT	ENSP00000245907.4:n.1687-147_1687-146insCT
ENST00000600763.1:n.320-147_320-146insCT
NM_000064.3:c.1687-147_1687-146insCT	NP_000055.2:n.1687-147_1687-146insCT
NM_000064.4:c.1687-147_1687-146insCT MANE Select	NP_000055.2:n.1687-147_1687-146insCT