Canonical Allele Identifier: CA2524981059

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710023_6710029del , CM000681.2:g.6710023_6710029del	GRCh38
NC_000019.9:g.6710034_6710040del , CM000681.1:g.6710034_6710040del	GRCh37
NC_000019.8:g.6661034_6661040del	NCBI36
NG_009557.1:g.15623_15629del , LRG_27:g.15623_15629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-187_1564-181del	ENSP00000512083.1:n.1564-187_1564-181del
ENST00000695654.1:c.811-187_811-181del	ENSP00000512085.1:n.811-187_811-181del
ENST00000695655.1:c.592-151_592-145del	ENSP00000512086.1:n.592-151_592-145del
ENST00000695692.1:n.1051-187_1051-181del
ENST00000245907.11:c.1687-187_1687-181del MANE Select	ENSP00000245907.4:n.1687-187_1687-181del
ENST00000245907.10:c.1687-187_1687-181del	ENSP00000245907.4:n.1687-187_1687-181del
ENST00000600763.1:n.320-187_320-181del
NM_000064.3:c.1687-187_1687-181del	NP_000055.2:n.1687-187_1687-181del
NM_000064.4:c.1687-187_1687-181del MANE Select	NP_000055.2:n.1687-187_1687-181del