Canonical Allele Identifier: CA2320566048

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709968_6709970delinsGGA , CM000681.2:g.6709968_6709970delinsGGA	GRCh38
NC_000019.9:g.6709979_6709981delinsGGA , CM000681.1:g.6709979_6709981delinsGGA	GRCh37
NC_000019.8:g.6660979_6660981delinsGGA	NCBI36
NG_009557.1:g.15682_15684delinsTCC , LRG_27:g.15682_15684delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-128_1564-126delinsTCC	ENSP00000512083.1:n.1564-128_1564-126delinsTCC
ENST00000695654.1:c.811-128_811-126delinsTCC	ENSP00000512085.1:n.811-128_811-126delinsTCC
ENST00000695655.1:c.592-92_592-90delinsTCC	ENSP00000512086.1:n.592-92_592-90delinsTCC
ENST00000695692.1:n.1051-128_1051-126delinsTCC
ENST00000245907.11:c.1687-128_1687-126delinsTCC MANE Select	ENSP00000245907.4:n.1687-128_1687-126delinsTCC
ENST00000245907.10:c.1687-128_1687-126delinsTCC	ENSP00000245907.4:n.1687-128_1687-126delinsTCC
ENST00000600763.1:n.320-128_320-126delinsTCC
NM_000064.3:c.1687-128_1687-126delinsTCC	NP_000055.2:n.1687-128_1687-126delinsTCC
NM_000064.4:c.1687-128_1687-126delinsTCC MANE Select	NP_000055.2:n.1687-128_1687-126delinsTCC