Canonical Allele Identifier: CA993073449

Gene: C3

Linked Data

• gnomAD v3: 19-6709993-G-GA
• gnomAD v4: 19-6709993-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709993_6709994insA , CM000681.2:g.6709993_6709994insA	GRCh38
NC_000019.9:g.6710004_6710005insA , CM000681.1:g.6710004_6710005insA	GRCh37
NC_000019.8:g.6661004_6661005insA	NCBI36
NG_009557.1:g.15658_15659insT , LRG_27:g.15658_15659insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-152_1564-151insT	ENSP00000512083.1:n.1564-152_1564-151insT
ENST00000695654.1:c.811-152_811-151insT	ENSP00000512085.1:n.811-152_811-151insT
ENST00000695655.1:c.592-116_592-115insT	ENSP00000512086.1:n.592-116_592-115insT
ENST00000695692.1:n.1051-152_1051-151insT
ENST00000245907.11:c.1687-152_1687-151insT MANE Select	ENSP00000245907.4:n.1687-152_1687-151insT
ENST00000245907.10:c.1687-152_1687-151insT	ENSP00000245907.4:n.1687-152_1687-151insT
ENST00000600763.1:n.320-152_320-151insT
NM_000064.3:c.1687-152_1687-151insT	NP_000055.2:n.1687-152_1687-151insT
NM_000064.4:c.1687-152_1687-151insT MANE Select	NP_000055.2:n.1687-152_1687-151insT