Canonical Allele Identifier: CA2587876920

Gene: C3

Linked Data

• gnomAD v4: 19-6709588-CCCCACTGCACTGCCCTCTCCAGTCCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709594_6709620del , CM000681.2:g.6709594_6709620del	GRCh38
NC_000019.9:g.6709605_6709631del , CM000681.1:g.6709605_6709631del	GRCh37
NC_000019.8:g.6660605_6660631del	NCBI36
NG_009557.1:g.16037_16063del , LRG_27:g.16037_16063del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+69_1722+95del	ENSP00000512083.1:n.1722+69_1722+95del
ENST00000695654.1:c.969+69_969+95del	ENSP00000512085.1:n.969+69_969+95del
ENST00000695655.1:c.786+69_786+95del	ENSP00000512086.1:n.786+69_786+95del
ENST00000695692.1:n.1209+69_1209+95del
ENST00000245907.11:c.1845+69_1845+95del MANE Select	ENSP00000245907.4:n.1845+69_1845+95del
ENST00000245907.10:c.1845+69_1845+95del	ENSP00000245907.4:n.1845+69_1845+95del
NM_000064.3:c.1845+69_1845+95del	NP_000055.2:n.1845+69_1845+95del
NM_000064.4:c.1845+69_1845+95del MANE Select	NP_000055.2:n.1845+69_1845+95del