Canonical Allele Identifier: CA2587877444

Gene: C3

Linked Data

• gnomAD v4: 19-6709632-C-CCCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709633_6709634insCCCCAC , CM000681.2:g.6709633_6709634insCCCCAC	GRCh38
NC_000019.9:g.6709644_6709645insCCCCAC , CM000681.1:g.6709644_6709645insCCCCAC	GRCh37
NC_000019.8:g.6660644_6660645insCCCCAC	NCBI36
NG_009557.1:g.16019_16020insTGGGGG , LRG_27:g.16019_16020insTGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+51_1722+52insTGGGGG	ENSP00000512083.1:n.1722+51_1722+52insTGGGGG
ENST00000695654.1:c.969+51_969+52insTGGGGG	ENSP00000512085.1:n.969+51_969+52insTGGGGG
ENST00000695655.1:c.786+51_786+52insTGGGGG	ENSP00000512086.1:n.786+51_786+52insTGGGGG
ENST00000695692.1:n.1209+51_1209+52insTGGGGG
ENST00000245907.11:c.1845+51_1845+52insTGGGGG MANE Select	ENSP00000245907.4:n.1845+51_1845+52insTGGGGG
ENST00000245907.10:c.1845+51_1845+52insTGGGGG	ENSP00000245907.4:n.1845+51_1845+52insTGGGGG
NM_000064.3:c.1845+51_1845+52insTGGGGG	NP_000055.2:n.1845+51_1845+52insTGGGGG
NM_000064.4:c.1845+51_1845+52insTGGGGG MANE Select	NP_000055.2:n.1845+51_1845+52insTGGGGG