Canonical Allele Identifier: CA2813446550

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709969dup , CM000681.2:g.6709969dup	GRCh38
NC_000019.9:g.6709980dup , CM000681.1:g.6709980dup	GRCh37
NC_000019.8:g.6660980dup	NCBI36
NG_009557.1:g.15687dup , LRG_27:g.15687dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-123dup	ENSP00000512083.1:n.1564-123dup
ENST00000695654.1:c.811-123dup	ENSP00000512085.1:n.811-123dup
ENST00000695655.1:c.592-87dup	ENSP00000512086.1:n.592-87dup
ENST00000695692.1:n.1051-123dup
ENST00000245907.11:c.1687-123dup MANE Select	ENSP00000245907.4:n.1687-123dup
ENST00000245907.10:c.1687-123dup	ENSP00000245907.4:n.1687-123dup
ENST00000600763.1:n.320-123dup
NM_000064.3:c.1687-123dup	NP_000055.2:n.1687-123dup
NM_000064.4:c.1687-123dup MANE Select	NP_000055.2:n.1687-123dup