Canonical Allele Identifier: CA2320551518

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681918_6681919delinsAG , CM000681.2:g.6681918_6681919delinsAG	GRCh38
NC_000019.9:g.6681929_6681930delinsAG , CM000681.1:g.6681929_6681930delinsAG	GRCh37
NC_000019.8:g.6632929_6632930delinsAG	NCBI36
NG_009557.1:g.43733_43734delinsCT , LRG_27:g.43733_43734delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2698+22_2698+23delinsCT
ENST00000695653.1:c.2259+22_2259+23delinsCT	ENSP00000512084.1:n.2259+22_2259+23delinsCT
ENST00000695654.1:c.3375+22_3375+23delinsCT	ENSP00000512085.1:n.3375+22_3375+23delinsCT
ENST00000695689.1:c.321+22_321+23delinsCT	ENSP00000512101.1:n.321+22_321+23delinsCT
ENST00000695690.1:n.563_564delinsCT
ENST00000695691.1:n.563_564delinsCT
ENST00000245907.11:c.4350+22_4350+23delinsCT MANE Select	ENSP00000245907.4:n.4350+22_4350+23delinsCT
ENST00000245907.10:c.4350+22_4350+23delinsCT	ENSP00000245907.4:n.4350+22_4350+23delinsCT
ENST00000596548.1:c.471+22_471+23delinsCT	ENSP00000469744.1:n.471+22_471+23delinsCT
ENST00000599899.5:n.1309+22_1309+23delinsCT
ENST00000601008.1:c.242-3961_242-3960delinsCT	ENSP00000471384.1:n.242-3961_242-3960delinsCT
NM_000064.3:c.4350+22_4350+23delinsCT	NP_000055.2:n.4350+22_4350+23delinsCT
NM_000064.4:c.4350+22_4350+23delinsCT MANE Select	NP_000055.2:n.4350+22_4350+23delinsCT