Canonical Allele Identifier: CA993073601

Gene: C3

Linked Data

• gnomAD v3: 19-6710024-GGCGGGAGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGA-G
• gnomAD v4: 19-6710024-GGCGGGAGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGGGGGAGAGAGGGAAAGGGAAAGAGGGAGAGAAAGGGAGAGGGAGAGAGAGGGAAAGAGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710026_6710178del , CM000681.2:g.6710026_6710178del	GRCh38
NC_000019.9:g.6710037_6710189del , CM000681.1:g.6710037_6710189del	GRCh37
NC_000019.8:g.6661037_6661189del	NCBI36
NG_009557.1:g.15475_15627del , LRG_27:g.15475_15627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-335_1564-183del	ENSP00000512083.1:n.1564-335_1564-183del
ENST00000695654.1:c.811-335_811-183del	ENSP00000512085.1:n.811-335_811-183del
ENST00000695655.1:c.592-299_592-147del	ENSP00000512086.1:n.592-299_592-147del
ENST00000695692.1:n.1051-335_1051-183del
ENST00000245907.11:c.1687-335_1687-183del MANE Select	ENSP00000245907.4:n.1687-335_1687-183del
ENST00000245907.10:c.1687-335_1687-183del	ENSP00000245907.4:n.1687-335_1687-183del
ENST00000600763.1:n.320-335_320-183del
NM_000064.3:c.1687-335_1687-183del	NP_000055.2:n.1687-335_1687-183del
NM_000064.4:c.1687-335_1687-183del MANE Select	NP_000055.2:n.1687-335_1687-183del