Canonical Allele Identifier: CA2560331168

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710039_6710040dup , CM000681.2:g.6710039_6710040dup	GRCh38
NC_000019.9:g.6710050_6710051dup , CM000681.1:g.6710050_6710051dup	GRCh37
NC_000019.8:g.6661050_6661051dup	NCBI36
NG_009557.1:g.15622_15623dup , LRG_27:g.15622_15623dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-188_1564-187dup	ENSP00000512083.1:n.1564-188_1564-187dup
ENST00000695654.1:c.811-188_811-187dup	ENSP00000512085.1:n.811-188_811-187dup
ENST00000695655.1:c.592-152_592-151dup	ENSP00000512086.1:n.592-152_592-151dup
ENST00000695692.1:n.1051-188_1051-187dup
ENST00000245907.11:c.1687-188_1687-187dup MANE Select	ENSP00000245907.4:n.1687-188_1687-187dup
ENST00000245907.10:c.1687-188_1687-187dup	ENSP00000245907.4:n.1687-188_1687-187dup
ENST00000600763.1:n.320-188_320-187dup
NM_000064.3:c.1687-188_1687-187dup	NP_000055.2:n.1687-188_1687-187dup
NM_000064.4:c.1687-188_1687-187dup MANE Select	NP_000055.2:n.1687-188_1687-187dup