Canonical Allele Identifier: CA2320566080

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710004_6710006delinsAGG , CM000681.2:g.6710004_6710006delinsAGG	GRCh38
NC_000019.9:g.6710015_6710017delinsAGG , CM000681.1:g.6710015_6710017delinsAGG	GRCh37
NC_000019.8:g.6661015_6661017delinsAGG	NCBI36
NG_009557.1:g.15646_15648delinsCCT , LRG_27:g.15646_15648delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-164_1564-162delinsCCT	ENSP00000512083.1:n.1564-164_1564-162delinsCCT
ENST00000695654.1:c.811-164_811-162delinsCCT	ENSP00000512085.1:n.811-164_811-162delinsCCT
ENST00000695655.1:c.592-128_592-126delinsCCT	ENSP00000512086.1:n.592-128_592-126delinsCCT
ENST00000695692.1:n.1051-164_1051-162delinsCCT
ENST00000245907.11:c.1687-164_1687-162delinsCCT MANE Select	ENSP00000245907.4:n.1687-164_1687-162delinsCCT
ENST00000245907.10:c.1687-164_1687-162delinsCCT	ENSP00000245907.4:n.1687-164_1687-162delinsCCT
ENST00000600763.1:n.320-164_320-162delinsCCT
NM_000064.3:c.1687-164_1687-162delinsCCT	NP_000055.2:n.1687-164_1687-162delinsCCT
NM_000064.4:c.1687-164_1687-162delinsCCT MANE Select	NP_000055.2:n.1687-164_1687-162delinsCCT