Canonical Allele Identifier: CA2320566124

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710049_6710051delinsGAC , CM000681.2:g.6710049_6710051delinsGAC	GRCh38
NC_000019.9:g.6710060_6710062delinsGAC , CM000681.1:g.6710060_6710062delinsGAC	GRCh37
NC_000019.8:g.6661060_6661062delinsGAC	NCBI36
NG_009557.1:g.15601_15603delinsGTC , LRG_27:g.15601_15603delinsGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-209_1564-207delinsGTC	ENSP00000512083.1:n.1564-209_1564-207delinsGTC
ENST00000695654.1:c.811-209_811-207delinsGTC	ENSP00000512085.1:n.811-209_811-207delinsGTC
ENST00000695655.1:c.592-173_592-171delinsGTC	ENSP00000512086.1:n.592-173_592-171delinsGTC
ENST00000695692.1:n.1051-209_1051-207delinsGTC
ENST00000245907.11:c.1687-209_1687-207delinsGTC MANE Select	ENSP00000245907.4:n.1687-209_1687-207delinsGTC
ENST00000245907.10:c.1687-209_1687-207delinsGTC	ENSP00000245907.4:n.1687-209_1687-207delinsGTC
ENST00000600763.1:n.320-209_320-207delinsGTC
NM_000064.3:c.1687-209_1687-207delinsGTC	NP_000055.2:n.1687-209_1687-207delinsGTC
NM_000064.4:c.1687-209_1687-207delinsGTC MANE Select	NP_000055.2:n.1687-209_1687-207delinsGTC