Canonical Allele Identifier: CA2587877496

Gene: C3

Linked Data

• gnomAD v4: 19-6709657-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709658_6709659del , CM000681.2:g.6709658_6709659del	GRCh38
NC_000019.9:g.6709669_6709670del , CM000681.1:g.6709669_6709670del	GRCh37
NC_000019.8:g.6660669_6660670del	NCBI36
NG_009557.1:g.15993_15994del , LRG_27:g.15993_15994del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+25_1722+26del	ENSP00000512083.1:n.1722+25_1722+26del
ENST00000695654.1:c.969+25_969+26del	ENSP00000512085.1:n.969+25_969+26del
ENST00000695655.1:c.786+25_786+26del	ENSP00000512086.1:n.786+25_786+26del
ENST00000695692.1:n.1209+25_1209+26del
ENST00000245907.11:c.1845+25_1845+26del MANE Select	ENSP00000245907.4:n.1845+25_1845+26del
ENST00000245907.10:c.1845+25_1845+26del	ENSP00000245907.4:n.1845+25_1845+26del
NM_000064.3:c.1845+25_1845+26del	NP_000055.2:n.1845+25_1845+26del
NM_000064.4:c.1845+25_1845+26del MANE Select	NP_000055.2:n.1845+25_1845+26del