Canonical Allele Identifier: CA2813446556

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710003_6710004insGGGGAGAGAGGGGGAGAGAGGG , CM000681.2:g.6710003_6710004insGGGGAGAGAGGGGGAGAGAGGG	GRCh38
NC_000019.9:g.6710014_6710015insGGGGAGAGAGGGGGAGAGAGGG , CM000681.1:g.6710014_6710015insGGGGAGAGAGGGGGAGAGAGGG	GRCh37
NC_000019.8:g.6661014_6661015insGGGGAGAGAGGGGGAGAGAGGG	NCBI36
NG_009557.1:g.15659_15660insCCTCTCTCCCCCCCTCTCTCCC , LRG_27:g.15659_15660insCCTCTCTCCCCCCCTCTCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-151_1564-150insCCTCTCTCCCCCCCTCTCTCCC	ENSP00000512083.1:n.1564-151_1564-150insCCTCTCTCCCCCCCTCTCTCC...
ENST00000695654.1:c.811-151_811-150insCCTCTCTCCCCCCCTCTCTCCC	ENSP00000512085.1:n.811-151_811-150insCCTCTCTCCCCCCCTCTCTCCC
ENST00000695655.1:c.592-115_592-114insCCTCTCTCCCCCCCTCTCTCCC	ENSP00000512086.1:n.592-115_592-114insCCTCTCTCCCCCCCTCTCTCCC
ENST00000695692.1:n.1051-151_1051-150insCCTCTCTCCCCCCCTCTCTCCC
ENST00000245907.11:c.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCCC MANE Select	ENSP00000245907.4:n.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCC...
ENST00000245907.10:c.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCCC	ENSP00000245907.4:n.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCC...
ENST00000600763.1:n.320-151_320-150insCCTCTCTCCCCCCCTCTCTCCC
NM_000064.3:c.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCCC	NP_000055.2:n.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCCC
NM_000064.4:c.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCCC MANE Select	NP_000055.2:n.1687-151_1687-150insCCTCTCTCCCCCCCTCTCTCCC