Canonical Allele Identifier: CA2320566085

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710006_6710018delinsGGAGAGAGAGGGA , CM000681.2:g.6710006_6710018delinsGGAGAGAGAGGGA	GRCh38
NC_000019.9:g.6710017_6710029delinsGGAGAGAGAGGGA , CM000681.1:g.6710017_6710029delinsGGAGAGAGAGGGA	GRCh37
NC_000019.8:g.6661017_6661029delinsGGAGAGAGAGGGA	NCBI36
NG_009557.1:g.15634_15646delinsTCCCTCTCTCTCC , LRG_27:g.15634_15646delinsTCCCTCTCTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-176_1564-164delinsTCCCTCTCTCTCC	ENSP00000512083.1:n.1564-176_1564-164delinsTCCCTCTCTCTCC
ENST00000695654.1:c.811-176_811-164delinsTCCCTCTCTCTCC	ENSP00000512085.1:n.811-176_811-164delinsTCCCTCTCTCTCC
ENST00000695655.1:c.592-140_592-128delinsTCCCTCTCTCTCC	ENSP00000512086.1:n.592-140_592-128delinsTCCCTCTCTCTCC
ENST00000695692.1:n.1051-176_1051-164delinsTCCCTCTCTCTCC
ENST00000245907.11:c.1687-176_1687-164delinsTCCCTCTCTCTCC MANE Select	ENSP00000245907.4:n.1687-176_1687-164delinsTCCCTCTCTCTCC
ENST00000245907.10:c.1687-176_1687-164delinsTCCCTCTCTCTCC	ENSP00000245907.4:n.1687-176_1687-164delinsTCCCTCTCTCTCC
ENST00000600763.1:n.320-176_320-164delinsTCCCTCTCTCTCC
NM_000064.3:c.1687-176_1687-164delinsTCCCTCTCTCTCC	NP_000055.2:n.1687-176_1687-164delinsTCCCTCTCTCTCC
NM_000064.4:c.1687-176_1687-164delinsTCCCTCTCTCTCC MANE Select	NP_000055.2:n.1687-176_1687-164delinsTCCCTCTCTCTCC