Canonical Allele Identifier: CA2320567784

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713107_6713108delinsAG , CM000681.2:g.6713107_6713108delinsAG	GRCh38
NC_000019.9:g.6713118_6713119delinsAG , CM000681.1:g.6713118_6713119delinsAG	GRCh37
NC_000019.8:g.6664118_6664119delinsAG	NCBI36
NG_009557.1:g.12544_12545delinsCT , LRG_27:g.12544_12545delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+81_880+82delinsCT	ENSP00000512083.1:n.880+81_880+82delinsCT
ENST00000695654.1:c.127+81_127+82delinsCT	ENSP00000512085.1:n.127+81_127+82delinsCT
ENST00000695692.1:n.327+81_327+82delinsCT
ENST00000245907.11:c.1003+81_1003+82delinsCT MANE Select	ENSP00000245907.4:n.1003+81_1003+82delinsCT
ENST00000245907.10:c.1003+81_1003+82delinsCT	ENSP00000245907.4:n.1003+81_1003+82delinsCT
ENST00000594270.5:n.127+81_127+82delinsCT
ENST00000595577.1:n.507+81_507+82delinsCT
ENST00000597442.5:n.253+81_253+82delinsCT
NM_000064.3:c.1003+81_1003+82delinsCT	NP_000055.2:n.1003+81_1003+82delinsCT
NM_000064.4:c.1003+81_1003+82delinsCT MANE Select	NP_000055.2:n.1003+81_1003+82delinsCT