Canonical Allele Identifier: CA2587877487

Gene: C3

Linked Data

• gnomAD v4: 19-6709652-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709653_6709654del , CM000681.2:g.6709653_6709654del	GRCh38
NC_000019.9:g.6709664_6709665del , CM000681.1:g.6709664_6709665del	GRCh37
NC_000019.8:g.6660664_6660665del	NCBI36
NG_009557.1:g.15998_15999del , LRG_27:g.15998_15999del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+30_1722+31del	ENSP00000512083.1:n.1722+30_1722+31del
ENST00000695654.1:c.969+30_969+31del	ENSP00000512085.1:n.969+30_969+31del
ENST00000695655.1:c.786+30_786+31del	ENSP00000512086.1:n.786+30_786+31del
ENST00000695692.1:n.1209+30_1209+31del
ENST00000245907.11:c.1845+30_1845+31del MANE Select	ENSP00000245907.4:n.1845+30_1845+31del
ENST00000245907.10:c.1845+30_1845+31del	ENSP00000245907.4:n.1845+30_1845+31del
NM_000064.3:c.1845+30_1845+31del	NP_000055.2:n.1845+30_1845+31del
NM_000064.4:c.1845+30_1845+31del MANE Select	NP_000055.2:n.1845+30_1845+31del