Canonical Allele Identifier: CA2541360157

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710029_6710045del , CM000681.2:g.6710029_6710045del	GRCh38
NC_000019.9:g.6710040_6710056del , CM000681.1:g.6710040_6710056del	GRCh37
NC_000019.8:g.6661040_6661056del	NCBI36
NG_009557.1:g.15609_15625del , LRG_27:g.15609_15625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-201_1564-185del	ENSP00000512083.1:n.1564-201_1564-185del
ENST00000695654.1:c.811-201_811-185del	ENSP00000512085.1:n.811-201_811-185del
ENST00000695655.1:c.592-165_592-149del	ENSP00000512086.1:n.592-165_592-149del
ENST00000695692.1:n.1051-201_1051-185del
ENST00000245907.11:c.1687-201_1687-185del MANE Select	ENSP00000245907.4:n.1687-201_1687-185del
ENST00000245907.10:c.1687-201_1687-185del	ENSP00000245907.4:n.1687-201_1687-185del
ENST00000600763.1:n.320-201_320-185del
NM_000064.3:c.1687-201_1687-185del	NP_000055.2:n.1687-201_1687-185del
NM_000064.4:c.1687-201_1687-185del MANE Select	NP_000055.2:n.1687-201_1687-185del