Canonical Allele Identifier: CA993073448

Gene: C3

Linked Data

• gnomAD v3: 19-6709992-AGGGAGAGAGGGAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGG-A
• gnomAD v4: 19-6709992-AGGGAGAGAGGGAGGGAGAGAGAGGGAGAGAGGGCGGGAGAGAGAGAGAAAGGGAGAGACAGGGAGAGAGACGGAGAGACAGGGAGAGAGGGAGAGAGACGGAGAGACAGAGAGAGGGAGAGTGAGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710005_6710131del , CM000681.2:g.6710005_6710131del	GRCh38
NC_000019.9:g.6710016_6710142del , CM000681.1:g.6710016_6710142del	GRCh37
NC_000019.8:g.6661016_6661142del	NCBI36
NG_009557.1:g.15533_15659del , LRG_27:g.15533_15659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-277_1564-151del	ENSP00000512083.1:n.1564-277_1564-151del
ENST00000695654.1:c.811-277_811-151del	ENSP00000512085.1:n.811-277_811-151del
ENST00000695655.1:c.592-241_592-115del	ENSP00000512086.1:n.592-241_592-115del
ENST00000695692.1:n.1051-277_1051-151del
ENST00000245907.11:c.1687-277_1687-151del MANE Select	ENSP00000245907.4:n.1687-277_1687-151del
ENST00000245907.10:c.1687-277_1687-151del	ENSP00000245907.4:n.1687-277_1687-151del
ENST00000600763.1:n.320-277_320-151del
NM_000064.3:c.1687-277_1687-151del	NP_000055.2:n.1687-277_1687-151del
NM_000064.4:c.1687-277_1687-151del MANE Select	NP_000055.2:n.1687-277_1687-151del