Canonical Allele Identifier: CA2320567733

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712986_6712987delinsTA , CM000681.2:g.6712986_6712987delinsTA	GRCh38
NC_000019.9:g.6712997_6712998delinsTA , CM000681.1:g.6712997_6712998delinsTA	GRCh37
NC_000019.8:g.6663997_6663998delinsTA	NCBI36
NG_009557.1:g.12665_12666delinsTA , LRG_27:g.12665_12666delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+202_880+203delinsTA	ENSP00000512083.1:n.880+202_880+203delinsTA
ENST00000695654.1:c.127+202_127+203delinsTA	ENSP00000512085.1:n.127+202_127+203delinsTA
ENST00000695692.1:n.327+202_327+203delinsTA
ENST00000245907.11:c.1003+202_1003+203delinsTA MANE Select	ENSP00000245907.4:n.1003+202_1003+203delinsTA
ENST00000245907.10:c.1003+202_1003+203delinsTA	ENSP00000245907.4:n.1003+202_1003+203delinsTA
ENST00000594270.5:n.127+202_127+203delinsTA
ENST00000595577.1:n.507+202_507+203delinsTA
ENST00000597442.5:n.253+202_253+203delinsTA
NM_000064.3:c.1003+202_1003+203delinsTA	NP_000055.2:n.1003+202_1003+203delinsTA
NM_000064.4:c.1003+202_1003+203delinsTA MANE Select	NP_000055.2:n.1003+202_1003+203delinsTA