Canonical Allele Identifier: CA2320566065

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709989_6709991delinsGAA , CM000681.2:g.6709989_6709991delinsGAA	GRCh38
NC_000019.9:g.6710000_6710002delinsGAA , CM000681.1:g.6710000_6710002delinsGAA	GRCh37
NC_000019.8:g.6661000_6661002delinsGAA	NCBI36
NG_009557.1:g.15661_15663delinsTTC , LRG_27:g.15661_15663delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-149_1564-147delinsTTC	ENSP00000512083.1:n.1564-149_1564-147delinsTTC
ENST00000695654.1:c.811-149_811-147delinsTTC	ENSP00000512085.1:n.811-149_811-147delinsTTC
ENST00000695655.1:c.592-113_592-111delinsTTC	ENSP00000512086.1:n.592-113_592-111delinsTTC
ENST00000695692.1:n.1051-149_1051-147delinsTTC
ENST00000245907.11:c.1687-149_1687-147delinsTTC MANE Select	ENSP00000245907.4:n.1687-149_1687-147delinsTTC
ENST00000245907.10:c.1687-149_1687-147delinsTTC	ENSP00000245907.4:n.1687-149_1687-147delinsTTC
ENST00000600763.1:n.320-149_320-147delinsTTC
NM_000064.3:c.1687-149_1687-147delinsTTC	NP_000055.2:n.1687-149_1687-147delinsTTC
NM_000064.4:c.1687-149_1687-147delinsTTC MANE Select	NP_000055.2:n.1687-149_1687-147delinsTTC