Canonical Allele Identifier: CA2552482866

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709992_6710005del , CM000681.2:g.6709992_6710005del	GRCh38
NC_000019.9:g.6710003_6710016del , CM000681.1:g.6710003_6710016del	GRCh37
NC_000019.8:g.6661003_6661016del	NCBI36
NG_009557.1:g.15647_15660del , LRG_27:g.15647_15660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-163_1564-150del	ENSP00000512083.1:n.1564-163_1564-150del
ENST00000695654.1:c.811-163_811-150del	ENSP00000512085.1:n.811-163_811-150del
ENST00000695655.1:c.592-127_592-114del	ENSP00000512086.1:n.592-127_592-114del
ENST00000695692.1:n.1051-163_1051-150del
ENST00000245907.11:c.1687-163_1687-150del MANE Select	ENSP00000245907.4:n.1687-163_1687-150del
ENST00000245907.10:c.1687-163_1687-150del	ENSP00000245907.4:n.1687-163_1687-150del
ENST00000600763.1:n.320-163_320-150del
NM_000064.3:c.1687-163_1687-150del	NP_000055.2:n.1687-163_1687-150del
NM_000064.4:c.1687-163_1687-150del MANE Select	NP_000055.2:n.1687-163_1687-150del