Canonical Allele Identifier: CA2320566074

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709994_6710008delinsGGAGAGAGGGAGGGA , CM000681.2:g.6709994_6710008delinsGGAGAGAGGGAGGGA	GRCh38
NC_000019.9:g.6710005_6710019delinsGGAGAGAGGGAGGGA , CM000681.1:g.6710005_6710019delinsGGAGAGAGGGAGGGA	GRCh37
NC_000019.8:g.6661005_6661019delinsGGAGAGAGGGAGGGA	NCBI36
NG_009557.1:g.15644_15658delinsTCCCTCCCTCTCTCC , LRG_27:g.15644_15658delinsTCCCTCCCTCTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-166_1564-152delinsTCCCTCCCTCTCTCC	ENSP00000512083.1:n.1564-166_1564-152delinsTCCCTCCCTCTCTCC
ENST00000695654.1:c.811-166_811-152delinsTCCCTCCCTCTCTCC	ENSP00000512085.1:n.811-166_811-152delinsTCCCTCCCTCTCTCC
ENST00000695655.1:c.592-130_592-116delinsTCCCTCCCTCTCTCC	ENSP00000512086.1:n.592-130_592-116delinsTCCCTCCCTCTCTCC
ENST00000695692.1:n.1051-166_1051-152delinsTCCCTCCCTCTCTCC
ENST00000245907.11:c.1687-166_1687-152delinsTCCCTCCCTCTCTCC MANE Select	ENSP00000245907.4:n.1687-166_1687-152delinsTCCCTCCCTCTCTCC
ENST00000245907.10:c.1687-166_1687-152delinsTCCCTCCCTCTCTCC	ENSP00000245907.4:n.1687-166_1687-152delinsTCCCTCCCTCTCTCC
ENST00000600763.1:n.320-166_320-152delinsTCCCTCCCTCTCTCC
NM_000064.3:c.1687-166_1687-152delinsTCCCTCCCTCTCTCC	NP_000055.2:n.1687-166_1687-152delinsTCCCTCCCTCTCTCC
NM_000064.4:c.1687-166_1687-152delinsTCCCTCCCTCTCTCC MANE Select	NP_000055.2:n.1687-166_1687-152delinsTCCCTCCCTCTCTCC