Canonical Allele Identifier: CA2587877451

Gene: C3

Linked Data

• gnomAD v4: 19-6709633-C-CCCCCCCCCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709633_6709634insCCCCCCCCCG , CM000681.2:g.6709633_6709634insCCCCCCCCCG	GRCh38
NC_000019.9:g.6709644_6709645insCCCCCCCCCG , CM000681.1:g.6709644_6709645insCCCCCCCCCG	GRCh37
NC_000019.8:g.6660644_6660645insCCCCCCCCCG	NCBI36
NG_009557.1:g.16018_16019insCGGGGGGGGG , LRG_27:g.16018_16019insCGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+50_1722+51insCGGGGGGGGG	ENSP00000512083.1:n.1722+50_1722+51insCGGGGGGGGG
ENST00000695654.1:c.969+50_969+51insCGGGGGGGGG	ENSP00000512085.1:n.969+50_969+51insCGGGGGGGGG
ENST00000695655.1:c.786+50_786+51insCGGGGGGGGG	ENSP00000512086.1:n.786+50_786+51insCGGGGGGGGG
ENST00000695692.1:n.1209+50_1209+51insCGGGGGGGGG
ENST00000245907.11:c.1845+50_1845+51insCGGGGGGGGG MANE Select	ENSP00000245907.4:n.1845+50_1845+51insCGGGGGGGGG
ENST00000245907.10:c.1845+50_1845+51insCGGGGGGGGG	ENSP00000245907.4:n.1845+50_1845+51insCGGGGGGGGG
NM_000064.3:c.1845+50_1845+51insCGGGGGGGGG	NP_000055.2:n.1845+50_1845+51insCGGGGGGGGG
NM_000064.4:c.1845+50_1845+51insCGGGGGGGGG MANE Select	NP_000055.2:n.1845+50_1845+51insCGGGGGGGGG