Canonical Allele Identifier: CA2320566130

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710051_6710052delinsCA , CM000681.2:g.6710051_6710052delinsCA	GRCh38
NC_000019.9:g.6710062_6710063delinsCA , CM000681.1:g.6710062_6710063delinsCA	GRCh37
NC_000019.8:g.6661062_6661063delinsCA	NCBI36
NG_009557.1:g.15600_15601delinsTG , LRG_27:g.15600_15601delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-210_1564-209delinsTG	ENSP00000512083.1:n.1564-210_1564-209delinsTG
ENST00000695654.1:c.811-210_811-209delinsTG	ENSP00000512085.1:n.811-210_811-209delinsTG
ENST00000695655.1:c.592-174_592-173delinsTG	ENSP00000512086.1:n.592-174_592-173delinsTG
ENST00000695692.1:n.1051-210_1051-209delinsTG
ENST00000245907.11:c.1687-210_1687-209delinsTG MANE Select	ENSP00000245907.4:n.1687-210_1687-209delinsTG
ENST00000245907.10:c.1687-210_1687-209delinsTG	ENSP00000245907.4:n.1687-210_1687-209delinsTG
ENST00000600763.1:n.320-210_320-209delinsTG
NM_000064.3:c.1687-210_1687-209delinsTG	NP_000055.2:n.1687-210_1687-209delinsTG
NM_000064.4:c.1687-210_1687-209delinsTG MANE Select	NP_000055.2:n.1687-210_1687-209delinsTG