Canonical Allele Identifier: CA2576592260

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709901_6709917del , CM000681.2:g.6709901_6709917del	GRCh38
NC_000019.9:g.6709912_6709928del , CM000681.1:g.6709912_6709928del	GRCh37
NC_000019.8:g.6660912_6660928del	NCBI36
NG_009557.1:g.15740_15756del , LRG_27:g.15740_15756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-70_1564-54del	ENSP00000512083.1:n.1564-70_1564-54del
ENST00000695654.1:c.811-70_811-54del	ENSP00000512085.1:n.811-70_811-54del
ENST00000695655.1:c.592-34_592-18del	ENSP00000512086.1:n.592-34_592-18del
ENST00000695692.1:n.1051-70_1051-54del
ENST00000245907.11:c.1687-70_1687-54del MANE Select	ENSP00000245907.4:n.1687-70_1687-54del
ENST00000245907.10:c.1687-70_1687-54del	ENSP00000245907.4:n.1687-70_1687-54del
ENST00000600763.1:n.320-70_320-54del
NM_000064.3:c.1687-70_1687-54del	NP_000055.2:n.1687-70_1687-54del
NM_000064.4:c.1687-70_1687-54del MANE Select	NP_000055.2:n.1687-70_1687-54del