Canonical Allele Identifier: CA2320566057

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709975_6709991delinsGAGGGAGAGAGAGAGAA , CM000681.2:g.6709975_6709991delinsGAGGGAGAGAGAGAGAA	GRCh38
NC_000019.9:g.6709986_6710002delinsGAGGGAGAGAGAGAGAA , CM000681.1:g.6709986_6710002delinsGAGGGAGAGAGAGAGAA	GRCh37
NC_000019.8:g.6660986_6661002delinsGAGGGAGAGAGAGAGAA	NCBI36
NG_009557.1:g.15661_15677delinsTTCTCTCTCTCTCCCTC , LRG_27:g.15661_15677delinsTTCTCTCTCTCTCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-149_1564-133delinsTTCTCTCTCTCTCCCTC	ENSP00000512083.1:n.1564-149_1564-133delinsTTCTCTCTCTCTCCCTC
ENST00000695654.1:c.811-149_811-133delinsTTCTCTCTCTCTCCCTC	ENSP00000512085.1:n.811-149_811-133delinsTTCTCTCTCTCTCCCTC
ENST00000695655.1:c.592-113_592-97delinsTTCTCTCTCTCTCCCTC	ENSP00000512086.1:n.592-113_592-97delinsTTCTCTCTCTCTCCCTC
ENST00000695692.1:n.1051-149_1051-133delinsTTCTCTCTCTCTCCCTC
ENST00000245907.11:c.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC MANE Select	ENSP00000245907.4:n.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC
ENST00000245907.10:c.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC	ENSP00000245907.4:n.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC
ENST00000600763.1:n.320-149_320-133delinsTTCTCTCTCTCTCCCTC
NM_000064.3:c.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC	NP_000055.2:n.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC
NM_000064.4:c.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC MANE Select	NP_000055.2:n.1687-149_1687-133delinsTTCTCTCTCTCTCCCTC