Canonical Allele Identifier: CA2587877413

Gene: C3

Linked Data

• gnomAD v4: 19-6709623-C-CCCCCCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709627_6709628insCAACCCC , CM000681.2:g.6709627_6709628insCAACCCC	GRCh38
NC_000019.9:g.6709638_6709639insCAACCCC , CM000681.1:g.6709638_6709639insCAACCCC	GRCh37
NC_000019.8:g.6660638_6660639insCAACCCC	NCBI36
NG_009557.1:g.16028_16029insTTGGGGG , LRG_27:g.16028_16029insTTGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1722+60_1722+61insTTGGGGG	ENSP00000512083.1:n.1722+60_1722+61insTTGGGGG
ENST00000695654.1:c.969+60_969+61insTTGGGGG	ENSP00000512085.1:n.969+60_969+61insTTGGGGG
ENST00000695655.1:c.786+60_786+61insTTGGGGG	ENSP00000512086.1:n.786+60_786+61insTTGGGGG
ENST00000695692.1:n.1209+60_1209+61insTTGGGGG
ENST00000245907.11:c.1845+60_1845+61insTTGGGGG MANE Select	ENSP00000245907.4:n.1845+60_1845+61insTTGGGGG
ENST00000245907.10:c.1845+60_1845+61insTTGGGGG	ENSP00000245907.4:n.1845+60_1845+61insTTGGGGG
NM_000064.3:c.1845+60_1845+61insTTGGGGG	NP_000055.2:n.1845+60_1845+61insTTGGGGG
NM_000064.4:c.1845+60_1845+61insTTGGGGG MANE Select	NP_000055.2:n.1845+60_1845+61insTTGGGGG