Canonical Allele Identifier: CA2587876969

Gene: C3

Linked Data

• gnomAD v4: 19-6709610-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709610_6709611insC , CM000681.2:g.6709610_6709611insC	GRCh38
NC_000019.9:g.6709621_6709622insC , CM000681.1:g.6709621_6709622insC	GRCh37
NC_000019.8:g.6660621_6660622insC	NCBI36
NG_009557.1:g.16041_16042insG , LRG_27:g.16041_16042insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+73_1722+74insG	ENSP00000512083.1:n.1722+73_1722+74insG
ENST00000695654.1:c.969+73_969+74insG	ENSP00000512085.1:n.969+73_969+74insG
ENST00000695655.1:c.786+73_786+74insG	ENSP00000512086.1:n.786+73_786+74insG
ENST00000695692.1:n.1209+73_1209+74insG
ENST00000245907.11:c.1845+73_1845+74insG MANE Select	ENSP00000245907.4:n.1845+73_1845+74insG
ENST00000245907.10:c.1845+73_1845+74insG	ENSP00000245907.4:n.1845+73_1845+74insG
NM_000064.3:c.1845+73_1845+74insG	NP_000055.2:n.1845+73_1845+74insG
NM_000064.4:c.1845+73_1845+74insG MANE Select	NP_000055.2:n.1845+73_1845+74insG