Canonical Allele Identifier: CA2320566108

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710035_6710041delinsGAGAGAA , CM000681.2:g.6710035_6710041delinsGAGAGAA	GRCh38
NC_000019.9:g.6710046_6710052delinsGAGAGAA , CM000681.1:g.6710046_6710052delinsGAGAGAA	GRCh37
NC_000019.8:g.6661046_6661052delinsGAGAGAA	NCBI36
NG_009557.1:g.15611_15617delinsTTCTCTC , LRG_27:g.15611_15617delinsTTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-199_1564-193delinsTTCTCTC	ENSP00000512083.1:n.1564-199_1564-193delinsTTCTCTC
ENST00000695654.1:c.811-199_811-193delinsTTCTCTC	ENSP00000512085.1:n.811-199_811-193delinsTTCTCTC
ENST00000695655.1:c.592-163_592-157delinsTTCTCTC	ENSP00000512086.1:n.592-163_592-157delinsTTCTCTC
ENST00000695692.1:n.1051-199_1051-193delinsTTCTCTC
ENST00000245907.11:c.1687-199_1687-193delinsTTCTCTC MANE Select	ENSP00000245907.4:n.1687-199_1687-193delinsTTCTCTC
ENST00000245907.10:c.1687-199_1687-193delinsTTCTCTC	ENSP00000245907.4:n.1687-199_1687-193delinsTTCTCTC
ENST00000600763.1:n.320-199_320-193delinsTTCTCTC
NM_000064.3:c.1687-199_1687-193delinsTTCTCTC	NP_000055.2:n.1687-199_1687-193delinsTTCTCTC
NM_000064.4:c.1687-199_1687-193delinsTTCTCTC MANE Select	NP_000055.2:n.1687-199_1687-193delinsTTCTCTC