Canonical Allele Identifier: CA2587877595

Gene: C3

Linked Data

• gnomAD v4: 19-6709960-GGGGAGGGGGAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709962_6709973del , CM000681.2:g.6709962_6709973del	GRCh38
NC_000019.9:g.6709973_6709984del , CM000681.1:g.6709973_6709984del	GRCh37
NC_000019.8:g.6660973_6660984del	NCBI36
NG_009557.1:g.15680_15691del , LRG_27:g.15680_15691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-130_1564-119del	ENSP00000512083.1:n.1564-130_1564-119del
ENST00000695654.1:c.811-130_811-119del	ENSP00000512085.1:n.811-130_811-119del
ENST00000695655.1:c.592-94_592-83del	ENSP00000512086.1:n.592-94_592-83del
ENST00000695692.1:n.1051-130_1051-119del
ENST00000245907.11:c.1687-130_1687-119del MANE Select	ENSP00000245907.4:n.1687-130_1687-119del
ENST00000245907.10:c.1687-130_1687-119del	ENSP00000245907.4:n.1687-130_1687-119del
ENST00000600763.1:n.320-130_320-119del
NM_000064.3:c.1687-130_1687-119del	NP_000055.2:n.1687-130_1687-119del
NM_000064.4:c.1687-130_1687-119del MANE Select	NP_000055.2:n.1687-130_1687-119del