Canonical Allele Identifier: CA2320566129

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710051_6710079delinsCAGGGAGAGAGACGGAGAGACAGGGAGAG , CM000681.2:g.6710051_6710079delinsCAGGGAGAGAGACGGAGAGACAGGGAGAG	GRCh38
NC_000019.9:g.6710062_6710090delinsCAGGGAGAGAGACGGAGAGACAGGGAGAG , CM000681.1:g.6710062_6710090delinsCAGGGAGAGAGACGGAGAGACAGGGAGAG	GRCh37
NC_000019.8:g.6661062_6661090delinsCAGGGAGAGAGACGGAGAGACAGGGAGAG	NCBI36
NG_009557.1:g.15573_15601delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG , LRG_27:g.15573_15601delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-237_1564-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG	ENSP00000512083.1:n.1564-237_1564-209delinsCTCTCCCTGTCTCTCCGT...
ENST00000695654.1:c.811-237_811-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG	ENSP00000512085.1:n.811-237_811-209delinsCTCTCCCTGTCTCTCCGTCT...
ENST00000695655.1:c.592-201_592-173delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG	ENSP00000512086.1:n.592-201_592-173delinsCTCTCCCTGTCTCTCCGTCT...
ENST00000695692.1:n.1051-237_1051-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG
ENST00000245907.11:c.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG MANE Select	ENSP00000245907.4:n.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGT...
ENST00000245907.10:c.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG	ENSP00000245907.4:n.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGT...
ENST00000600763.1:n.320-237_320-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG
NM_000064.3:c.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG	NP_000055.2:n.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGTCTCTCT...
NM_000064.4:c.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGTCTCTCTCCCTG MANE Select	NP_000055.2:n.1687-237_1687-209delinsCTCTCCCTGTCTCTCCGTCTCTCT...