Canonical Allele Identifier: CA2813446565

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710033_6710034insGGAA , CM000681.2:g.6710033_6710034insGGAA	GRCh38
NC_000019.9:g.6710044_6710045insGGAA , CM000681.1:g.6710044_6710045insGGAA	GRCh37
NC_000019.8:g.6661044_6661045insGGAA	NCBI36
NG_009557.1:g.15618_15619insTTCC , LRG_27:g.15618_15619insTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-192_1564-191insTTCC	ENSP00000512083.1:n.1564-192_1564-191insTTCC
ENST00000695654.1:c.811-192_811-191insTTCC	ENSP00000512085.1:n.811-192_811-191insTTCC
ENST00000695655.1:c.592-156_592-155insTTCC	ENSP00000512086.1:n.592-156_592-155insTTCC
ENST00000695692.1:n.1051-192_1051-191insTTCC
ENST00000245907.11:c.1687-192_1687-191insTTCC MANE Select	ENSP00000245907.4:n.1687-192_1687-191insTTCC
ENST00000245907.10:c.1687-192_1687-191insTTCC	ENSP00000245907.4:n.1687-192_1687-191insTTCC
ENST00000600763.1:n.320-192_320-191insTTCC
NM_000064.3:c.1687-192_1687-191insTTCC	NP_000055.2:n.1687-192_1687-191insTTCC
NM_000064.4:c.1687-192_1687-191insTTCC MANE Select	NP_000055.2:n.1687-192_1687-191insTTCC