Canonical Allele Identifier: CA2320566099

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710041delinsGCGGGAGAGAGAGAGAA , CM000681.2:g.6710025_6710041delinsGCGGGAGAGAGAGAGAA	GRCh38
NC_000019.9:g.6710036_6710052delinsGCGGGAGAGAGAGAGAA , CM000681.1:g.6710036_6710052delinsGCGGGAGAGAGAGAGAA	GRCh37
NC_000019.8:g.6661036_6661052delinsGCGGGAGAGAGAGAGAA	NCBI36
NG_009557.1:g.15611_15627delinsTTCTCTCTCTCTCCCGC , LRG_27:g.15611_15627delinsTTCTCTCTCTCTCCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-199_1564-183delinsTTCTCTCTCTCTCCCGC	ENSP00000512083.1:n.1564-199_1564-183delinsTTCTCTCTCTCTCCCGC
ENST00000695654.1:c.811-199_811-183delinsTTCTCTCTCTCTCCCGC	ENSP00000512085.1:n.811-199_811-183delinsTTCTCTCTCTCTCCCGC
ENST00000695655.1:c.592-163_592-147delinsTTCTCTCTCTCTCCCGC	ENSP00000512086.1:n.592-163_592-147delinsTTCTCTCTCTCTCCCGC
ENST00000695692.1:n.1051-199_1051-183delinsTTCTCTCTCTCTCCCGC
ENST00000245907.11:c.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC MANE Select	ENSP00000245907.4:n.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC
ENST00000245907.10:c.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC	ENSP00000245907.4:n.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC
ENST00000600763.1:n.320-199_320-183delinsTTCTCTCTCTCTCCCGC
NM_000064.3:c.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC	NP_000055.2:n.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC
NM_000064.4:c.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC MANE Select	NP_000055.2:n.1687-199_1687-183delinsTTCTCTCTCTCTCCCGC