Canonical Allele Identifier: CA2320566105

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710028_6710032delinsGGAGA , CM000681.2:g.6710028_6710032delinsGGAGA	GRCh38
NC_000019.9:g.6710039_6710043delinsGGAGA , CM000681.1:g.6710039_6710043delinsGGAGA	GRCh37
NC_000019.8:g.6661039_6661043delinsGGAGA	NCBI36
NG_009557.1:g.15620_15624delinsTCTCC , LRG_27:g.15620_15624delinsTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-190_1564-186delinsTCTCC	ENSP00000512083.1:n.1564-190_1564-186delinsTCTCC
ENST00000695654.1:c.811-190_811-186delinsTCTCC	ENSP00000512085.1:n.811-190_811-186delinsTCTCC
ENST00000695655.1:c.592-154_592-150delinsTCTCC	ENSP00000512086.1:n.592-154_592-150delinsTCTCC
ENST00000695692.1:n.1051-190_1051-186delinsTCTCC
ENST00000245907.11:c.1687-190_1687-186delinsTCTCC MANE Select	ENSP00000245907.4:n.1687-190_1687-186delinsTCTCC
ENST00000245907.10:c.1687-190_1687-186delinsTCTCC	ENSP00000245907.4:n.1687-190_1687-186delinsTCTCC
ENST00000600763.1:n.320-190_320-186delinsTCTCC
NM_000064.3:c.1687-190_1687-186delinsTCTCC	NP_000055.2:n.1687-190_1687-186delinsTCTCC
NM_000064.4:c.1687-190_1687-186delinsTCTCC MANE Select	NP_000055.2:n.1687-190_1687-186delinsTCTCC