Canonical Allele Identifier: CA2515677439

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710026_6710156del , CM000681.2:g.6710026_6710156del	GRCh38
NC_000019.9:g.6710037_6710167del , CM000681.1:g.6710037_6710167del	GRCh37
NC_000019.8:g.6661037_6661167del	NCBI36
NG_009557.1:g.15497_15627del , LRG_27:g.15497_15627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-313_1564-183del	ENSP00000512083.1:n.1564-313_1564-183del
ENST00000695654.1:c.811-313_811-183del	ENSP00000512085.1:n.811-313_811-183del
ENST00000695655.1:c.592-277_592-147del	ENSP00000512086.1:n.592-277_592-147del
ENST00000695692.1:n.1051-313_1051-183del
ENST00000245907.11:c.1687-313_1687-183del MANE Select	ENSP00000245907.4:n.1687-313_1687-183del
ENST00000245907.10:c.1687-313_1687-183del	ENSP00000245907.4:n.1687-313_1687-183del
ENST00000600763.1:n.320-313_320-183del
NM_000064.3:c.1687-313_1687-183del	NP_000055.2:n.1687-313_1687-183del
NM_000064.4:c.1687-313_1687-183del MANE Select	NP_000055.2:n.1687-313_1687-183del