Canonical Allele Identifier: CA2830560107

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686317_6686318insGGA , CM000681.2:g.6686317_6686318insGGA	GRCh38
NC_000019.9:g.6686328_6686329insGGA , CM000681.1:g.6686328_6686329insGGA	GRCh37
NC_000019.8:g.6637328_6637329insGGA	NCBI36
NG_009557.1:g.39334_39335insTCC , LRG_27:g.39334_39335insTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-31_1995-30insTCC
ENST00000695652.1:c.3524-31_3524-30insTCC	ENSP00000512083.1:n.3524-31_3524-30insTCC
ENST00000695653.1:c.1556-31_1556-30insTCC	ENSP00000512084.1:n.1556-31_1556-30insTCC
ENST00000695654.1:c.2672-31_2672-30insTCC	ENSP00000512085.1:n.2672-31_2672-30insTCC
ENST00000695655.1:c.2588-31_2588-30insTCC	ENSP00000512086.1:n.2588-31_2588-30insTCC
ENST00000695692.1:n.3011-31_3011-30insTCC
ENST00000245907.11:c.3647-31_3647-30insTCC MANE Select	ENSP00000245907.4:n.3647-31_3647-30insTCC
ENST00000245907.10:c.3647-31_3647-30insTCC	ENSP00000245907.4:n.3647-31_3647-30insTCC
ENST00000596238.1:n.59_60insTCC
ENST00000598805.2:n.844_845insTCC
ENST00000601008.1:c.241+428_241+429insTCC	ENSP00000471384.1:n.241+428_241+429insTCC
NM_000064.3:c.3647-31_3647-30insTCC	NP_000055.2:n.3647-31_3647-30insTCC
NM_000064.4:c.3647-31_3647-30insTCC MANE Select	NP_000055.2:n.3647-31_3647-30insTCC